3,5-Bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzenamine

Frank Osterod; Arno Kraft

doi:10.3390/M115

and

Department of Organic Chemistry and Macromolecular Chemistry II, University of Düsseldorf, Universitätsstr. 1, D-40225 Düsseldorf, Germany

^*

Author to whom correspondence should be addressed.

^*

New address: Department of Chemistry, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK.

Molecules1999, 4(10), M115;https://doi.org/10.3390/M115

This article belongs to the Section Molbank Section of Molecules, 1997-2001

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The reduction was carried out as described in reference [1] by using a mixture of sulfur (7.10 g, 0.22 mol), Na₂S — 9 H₂O (240 g, 0.22 mol), water (140 mL) and pyridine (20 mL). A solution of this reducing agent (60 mL) was added to a solution of 3,5-bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]nitrobenzene (1) (1.00 g, 1.9 mmol) in warm pyridine (10 mL). The reaction mixture was heated to reflux for 90 min, during which time a yellow precipitate separated. The mixture was filtered and the filtrate was added dropwise to water (200 mL). The precipitate was collected by suction filtration and dried. The combined solids were extracted with chloroform, the solution was filtered and concentrated in vacuum to yield 2 as a light yellow solid (260 mg, 28%). The yield was not optimised [2].

Mp. : 291-293°C.

IR (KBr): 3357s; 2964s; 1616m; 1543m; 1495s; 1464m; 1458m; 1114w; 1011w; 842w; 726w.

¹H NMR (CDCl₃:DMSO-d₆ 6:1, 300 MHz): 8.09 (t, J = 1.4 Hz, 1 H, C6H3); 8.09 (AA′XX′, 4 H, C₆H₄); 7.65 (d, J = 1.4 Hz, 2 H, C₆H₃); 7.59 (AA′XX′, 4 H, C₆H₄); 4.92 (br. s, 2 H, NH₂); 1.39 (s, 18 H, CH₃).

¹³C NMR (CDCl₃:DMSO-d₆ 7:3, 125 MHz): 164.4; 163.8; 155.2; 149.4; 126.6; 126.04; 126.0; 125.2; 120.7; 114.8; 34.9; 31.0.

CI-MS (NH₃) : 512 (35); 511 (100, M+NH₄⁺); 495 (28); 494 (78, M+H⁺); 194 (36); 177 (28).

Reference and Notes

Krasovitskii, B. M.; Matskevich, R. M.; Malt'seva, N. I. J. Gen. Chem. USSR 1961, 2107.
The reduction procedure worked reasonably well and provided the only successful way to the amine. Other reduction conditions [formic acid, NEt₃, Pd/C; hydrazine hydrate, Raney-Ni; carbon monoxide, SnCl₄, PtCl₂(PPh₃)₂, dioxane] failed completely. However, considerable amounts of H₂S evolved during the reaction; because of the stench involved, we decided in the end not to repeat the procedure a second time.

Sample availability: available from the authors.

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