Unexpected Metal-Free Dehydrogenation of a β -Ketoester to a Phenol Using a Recyclable Oxoammonium Salt Unexpected Metal-Free Dehydrogenation of a β -Ketoester to a Phenol Using a Recyclable Oxoammonium Salt Unexpected Metal-Free Dehydrogenation of a β -Ketoester to a Phenol Using a Recyclable Oxoammonium Salt

: The conversion of ethyl 2-oxocyclohexanecarboxylate to ethyl salicylate using an oxoammonium salt is reported. The dehydrogenation reaction is operationally simple and compares favorably with previous literature examples for the same transformation and expands the scope of oxoammonium salts as reagents for oxidative functionalization processes. Abstract: The conversion of ethyl 2-oxocyclohexanecarboxylate to ethyl salicylate using an oxoammonium salt is reported. The dehydrogenation reaction is operationally simple and compares favorably with previous literature examples for the same transformation and expands the scope of oxoammonium salts as reagents for oxidative functionalization processes. Abstract: The conversion of ethyl 2-oxocyclohexanecarboxylate to ethyl salicylate using an oxoammonium salt is reported. The dehydrogenation reaction is operationally simple and compares favorably with previous literature examples for the same transformation and expands the scope of oxoammonium salts as reagents for oxidative functionalization processes.

In an attempt to expand the scope of previous methodologies, we sought to use 1 for the dehydrogenation of a range of cyclohexanones. This transformation is traditionally performed using hypervalent iodine reagents [30] or by palladium catalysis [31]. We wanted to see if 1 could be used as an environmentally benign alternative. As a sharpening stone for probing this reaction, our attention focused on ethyl 2-oxocyclohexanecarboxylate, 4, as a substrate. However, rather than obtaining ethyl 2-oxo-3-cyclohexene-1-carboxylate, 5, as the product, we observed the formation of ethyl salicylate, 6, a well-known phenolic compound (Scheme 2) [32][33][34][35][36]. We report this serendipitous discovery here.
Molbank 2020, 2020, x FOR PEER REVIEW 2 of 5 Ene-triketones have been prepared by oxidation of diketones [25], and perfluoroalkyl ketones can be converted to their α,β-unsaturated analogs [26]. Reactions are performed in the presence of a nitrogenous base such as pyridine or 2,6-dimethylpyridine (2,6lutidine). A superstoichiometric quantity of the oxoammonium salt is required because, in the presence of a base, the hydroxyammonium byproduct, 2, initially formed undergoes a comproportionation reaction with a further aliquot of 1 to generate two equivalents of nitroxide 3 [27,28]. Thus, a sacrificial equivalent of 1 is required in order to affect complete dehydrogenation of the substrate. The spent oxidant can be easily removed by filtration at the end of a reaction and converted back to 1 [29].
In an attempt to expand the scope of previous methodologies, we sought to use 1 for the dehydrogenation of a range of cyclohexanones. This transformation is traditionally performed using hypervalent iodine reagents [30] or by palladium catalysis [31]. We wanted to see if 1 could be used as an environmentally benign alternative. As a sharpening stone for probing this reaction, our attention focused on ethyl 2-oxocyclohexanecarboxylate, 4, as a substrate. However, rather than obtaining ethyl 2-oxo-3-cyclohexene-1-carboxylate, 5, as the product, we observed the formation of ethyl salicylate, 6, a well-known phenolic compound (Scheme 2) [32][33][34][35][36]. We report this serendipitous discovery here.

Results and Discussion
Our discovery arose when we performed the reaction of 4 with 3.6 eq. of 1, using 5 eq. of 2,6-lutidine as a base. Heating an acetonitrile solution of the reagents at 50 °C for 96 h led to an almost equimolar ratio of phenol 6 and unreacted starting material 4 ( Table 1, entry 1). Increasing the loading of 1 to 7.5 eq. and reducing the reaction time to 24 h, resulted in complete conversion to 6 (entry 2). Performing the reaction in absence of 2,6lutidine was not successful, indicating the importance of the base (entry 3). Reducing the reaction temperature to 25 °C slowed the reaction considerably, it taking 72 h to reach completion (entries 4 and 5). Operating at 50 °C but reducing the oxoammonium salt loading to 5 eq. required extending the reaction time to 72 h (entry 6). Attempts to perform the reaction catalytically in 1 using a number of secondary oxidants were not successful. In order to improve the efficacy of the stoichiometric protocol, we wanted to reduce the reaction time. To achieve this, we turned to using microwave heating under sealed-vessel conditions as a tool. This way we were able to reach 100 °C simply and safely and could reduce the reaction time from 24 h to 30 min and obtain a near-quantitative conversion (entry 7). These became the optimal conditions for the protocol.
Our attention turned next to the isolation of the phenol from the product mixture. With an organic base and byproducts from the oxoammonium salt in the mixture, isolation of 6 involved a series of extractions. The product mixture was first diluted with water and then dilute hydrochloric acid added. An extraction with petroleum ether removed non-acidic byproducts. The organic layer was then washed with dilute sodium hydroxide in order to extract the product as the phenoxide anion into the aqueous phase and leaving organic byproducts, spent oxidant, and any unreacted starting material in the organic phase. Acidification of the aqueous extract with dilute hydrochloric acid liberated the phenol which was then extracted using petroleum ether. Removal of the solvent gave 6 in 40% isolated yield.

Results and Discussion
Our discovery arose when we performed the reaction of 4 with 3.6 eq. of 1, using 5 eq. of 2,6-lutidine as a base. Heating an acetonitrile solution of the reagents at 50 • C for 96 h led to an almost equimolar ratio of phenol 6 and unreacted starting material 4 ( Table 1, entry 1). Increasing the loading of 1 to 7.5 eq. and reducing the reaction time to 24 h, resulted in complete conversion to 6 (entry 2). Performing the reaction in absence of 2,6-lutidine was not successful, indicating the importance of the base (entry 3). Reducing the reaction temperature to 25 • C slowed the reaction considerably, it taking 72 h to reach completion (entries 4 and 5). Operating at 50 • C but reducing the oxoammonium salt loading to 5 eq. required extending the reaction time to 72 h (entry 6). Attempts to perform the reaction catalytically in 1 using a number of secondary oxidants were not successful. In order to improve the efficacy of the stoichiometric protocol, we wanted to reduce the reaction time. To achieve this, we turned to using microwave heating under sealed-vessel conditions as a tool. This way we were able to reach 100 • C simply and safely and could reduce the reaction time from 24 h to 30 min and obtain a near-quantitative conversion (entry 7). These became the optimal conditions for the protocol.
Our attention turned next to the isolation of the phenol from the product mixture. With an organic base and byproducts from the oxoammonium salt in the mixture, isolation of 6 involved a series of extractions. The product mixture was first diluted with water and then dilute hydrochloric acid added. An extraction with petroleum ether removed non-acidic byproducts. The organic layer was then washed with dilute sodium hydroxide in order to extract the product as the phenoxide anion into the aqueous phase and leaving organic byproducts, spent oxidant, and any unreacted starting material in the organic phase. Acidification of the aqueous extract with dilute hydrochloric acid liberated the phenol which was then extracted using petroleum ether. Removal of the solvent gave 6 in 40% isolated yield.  The fact that phenol 6 is formed in the reaction of 4 with 1 is noteworthy in light of the two other literature reports of this transformation. One employs an o-iodoxybenzoic acid derivative bearing a trimethylammonium group [30]. A comparable yield of 6 is obtained in the oxidative dehydrogenation of 4. The other approach involves the use of 10 mol% of palladium chloride in conjunction with 2 eq. of chloranil as a terminal oxidant [31]. The phenol product is obtained in 95% yield after 18 h. Compared to these reports, our methodology has the advantage that it is metal-free and that the oxidant is cheaper, easier to use, recyclable, and non-toxic.

General
All microwave-heating reactions were performed using a CEM Discover SP microwave unit (CEM Corporation, Matthews, NC, USA), in closed-vessel configuration. Temperature was measured by means of an IR temperature sensor located below the reaction vessel. NMR spectra ( 1 H, 13 C) were obtained in deuterated chloroform at 300 K using a Brüker DRX-400 400 MHz spectrometer (Brüker, Billerica, MA, USA). 1 H-NMR spectra were referenced to residual CHCl 3 (7.26 ppm) in CDCl 3 . 13 C-NMR spectra were referenced to CDCl 3 (77.16 ppm). Reactions were monitored by an Agilent Technologies (Santa Clara, CA, USA) 7820A Gas Chromatograph attached to a 5975 Mass Spectrometer.

Synthesis of Ethyl Salicylate (6) [CAS 118-61-6]
Ethyl 2-oxocyclohexanecarboxylate [CAS 1655-07-8] (4, 1 mmol, 1 eq), 2,6-lutidine [CAS 108-48-5] (5 mmol, 5 eq), 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate (1, 7.5 mmol, 7.5 eq), acetonitrile (3 mL) and deionized water (1 mL) were added to a 40 mL-capacity glass tube equipped with a magnetic stir bar. The reaction mixture was sealed with a cap and placed into a CEM Discover SP microwave unit. The content of the vessel was heated to 100 • C and held at this temperature for 30 min, the microwave power automatically fluctuating to hold the reaction mixture at the desired temperature. The reaction mixture was stirred constantly. After the allotted time, the reaction mixture was allowed to cool to below 50 • C before taking the vessel out of the microwave unit. An intensely colored solution was obtained at this point. The product mixture was transferred from the glass tube to a separatory funnel whereupon water (2 mL) was added, followed by 1 M HCl (5 mL). An extraction with petroleum ether was performed (5 × 10 mL) in order to remove non-acidic byproducts. The organic layer was then washed with 0.5 M NaOH (2 × 25 mL) in order to extract the product in phenoxide anion form. At this point the color of the solution changed from yellow to green. The two basic aqueous fractions were collected and acidified with 2 M HCl until a pH of less than 3 was reached (~30 mL acid). At this point the solution turned a cloudy yellow color. This solution was extracted with petroleum ether (3 × 30 mL). The combined organic extracts were washed with brine (~30 mL) and dried over Na 2 SO 4 . The solvent was removed under reduced pressure by rotary evaporation affording pure phenol 6 as a yellow oil (66 mg, 40%). 1 (28), 120 (100), 92 (37), 65 (11). Spectral data for this compound are consistent with those previously reported [37,38] (Supplementary Materials).

Conclusions
In summary, we report the conversion of β-ketoester 4 to a phenol 6 using oxoammonium salt 1. The reaction is operationally simple and compares favorably with previous literature examples for the same transformation. This serendipitous discovery opens the door to further exploration of the dehydrogenation of ketones to generate phenol products and work is currently underway in our laboratory to this end.