12H-Dibenzo[d,g][1,2,3]triselenocin-12-ol

Abstract

Reaction of diphenylmethanol (4) with n-butyllithium and subsequent treatment with selenium resulted in 12H-dibenzo[d,g][1,2,3]triselenocin-12-ol (5) comprising a novel heterocyclic ring system. The title compound 5 was analyzed by ¹H-NMR, ¹³C-NMR and HPLC. Additionally, the structure of 5 was confirmed by single crystal X-ray diffraction.

1. Introduction

Examples of cyclic di- and triselenides are underrepresented in the literature. E.g., dibenzotriselenonine 1 has been synthesized by reaction of selenium with (Z)-2,3-bis(2-lithiophenyl)-2-butene (Figure 1) [1]. Dibenzodiselenocines 2 and 3 have been investigated as chiral selenium-π-acid catalysts for the asymmetric, oxidative functionalization of alkenes [2]. During our studies to synthesize novel selenium-containing heterocycles, we aimed to insert selenium into ortho-lithiated diphenylmethanol by an oxidative ring closing reaction.

2. Results and Discussion

2.1. Chemistry

The title compound 12H-dibenzo[d,g][1,2,3]triselenocin-12-ol (5) was synthesized by n-butyllithium-promoted directed ortho-lithiation of diphenylmethanol (4) under argon atmosphere and treatment with elemental selenium according to a modified literature protocol (Scheme 1) [2]. Compound 5 was obtained in low yield (18%) and its chemical structure was determined by ¹H-nuclear magnetic resonance spectroscopy (¹H-NMR) (Figure S1, Supplementary Materials), ¹³C-NMR (Figure S2, Supplementary Materials) and single crystal X-ray diffraction (Figure 2). The purity of compound 5 was analyzed by high performance liquid chromatography (HPLC) (Figure S3, Supplementary Materials).

2.2. X-ray Structure

The crystal packing of 5 features numerous hydrogen bonds, generating a three-dimensional network (Figure 3). The hydrogen atoms on the hydroxyl groups are 50% disordered, thus intermolecular hydrogen bonds are observed both in between hydroxyl groups and between hydroxyl groups and selenium atoms. The two aromatic rings form a dihedral angle of 65.3(2)°.

3. Materials and Methods

3.1. General

All reagents and solvents were of commercial quality and utilized without further purification. The purity of the title compound 5 was determined by reverse phase HPLC. An Agilent 1100 Series HPLC system (Agilent Technologies, Santa Clara, CA, USA) was used, equipped with an ultraviolet diode array detector (detection at 254 nm). The chromatographic separation was performed on an XBridge^TM C18 column (150 × 4.6 mm, 5 µm) from Waters (Milford, MA, USA). The injection volume was 5 μL and the flow 1.5 mL/min using the following gradient: 0.01 M KH₂PO₄, pH 2.3 (mobile phase A), MeOH (mobile phase B), 40% B to 85% B in 8 min; 85% B for 5 min; 85% B to 40% B in 2 min; stop time 16 min. Column chromatography was performed on Geduran Si₆₀ 40–63 µm silica from Merck (Darmstadt, Germany) or commercial 50 µm silica columns from Interchim (Montluçon, France) using an Interchim PuriFlash XS520Plus automated flash chromatography system. NMR spectra were measured on an Avance 300 MHz NMR spectrometer from Bruker (Billerica, MA, USA). Chemical shifts are reported in parts per million (ppm) relative to tetramethylsilane. All spectra were calibrated against the (residual proton) peak of the deuterated solvent used. X-ray diffraction data were collected on a STOE IPDS 2T diffractometer (STOE & Cie, Darmstadt, Germany) using monochromated Mo Kα radiation (0.71073 Å).

3.2. Chemistry

Synthesis of 12H-Dibenzo[d,g][1,2,3]triselenocin-12-ol (5)

In a 100 mL three-neck round bottom flask diphenylmethanol (4) (0.5 g, 2.71 mmol, 1 eq.) was dissolved in dry n-hexane (12.5 mL) and dry diethyl ether (9 mL) under an argon atmosphere. n-Butyllithium (8.5 mL of a 1.6 M solution in n-hexane, 13.6 mmol, 5 eq.) was added dropwise and the mixture was stirred for 16 h at 50 °C. During the reaction, a white solid precipitated and the color of the suspension changed to purple. After cooling to room temperature, selenium (1.0 g, 13.6 mmol, 5 eq.) and dry THF (9 mL) were added, and the suspension was stirred for 1.5 h under an argon atmosphere at 50 °C. The color changed from purple to yellow. After cooling to room temperature, the mixture was poured into ice water and stirred for 1 h under aerobic conditions. The mixture was extracted with dichloromethane (DCM) (three times) and the combined organic phases were washed with water (three times), dried over MgSO₄ and evaporated. The residue was purified twice by flash column chromatography (SiO₂, petroleum ether/ethyl acetate gradient elution from 0% to 25%, and petroleum ether/DCM gradient elution from 50% to 90%) to yield 210 mg (18%) of the title compound as a yellowish solid. ¹H-NMR (300 MHz, DMSO-d₆) δ 8.24–8.13 (dd, J = 8.0 Hz, 1.3 Hz, 2H), 7.70–7.62 (dd, J = 7.7 Hz, 1.3 Hz, 2H), 7.55–7.45 (td, J = 7.9 Hz, 1.3 Hz, 2H), 7.24–7.15 (td, J = 7.5 Hz, 1.5 Hz, 2H), 6.55 (s, 1H), 6.35 (s, 1H); ¹³C-NMR (75 MHz, DMSO-d₆) δ 152.0, 135.2, 130.2, 129.7, 129.4, 127.4, 72.3; HPLC: t_R = 9.27 min (purity 95.7%).

Crystal data for C₁₃H₁₀OSe₃ (M = 419.09 g·mol⁻¹): triclinic space group P-1(2), a = 7.4876(6) Å, b = 7.4939(5) Å, c = 12.4930(9) Å, V = 623.66(9) ų, Z = 2, T = 120(2) K, µ(MoKα) = 8.825 mm⁻¹, D_calc = 2.232 Mg m⁻³, 12,850 reflections measured (2.96° ≤ Θ ≤ 28.40°), 2960 unique (R_int = 0.0206, R1 = 0.0360) which were used in all calculations. CCDC 2184462 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html (accessed on 15 July 2022).

4. Conclusions

To the best of our knowledge, we report for the first time an example of a compound having a heterocyclic triselenocine core. The synthesis of 12H-dibenzo[d,g][1,2,3]triselenocin-12-ol (5) was performed by reaction of diphenylmethanol (4) with n-butyllithium and subsequent treatment with elemental selenium. The analytical characterization of the novel compound 5 comprised ¹H-NMR, ¹³C-NMR, HPLC, and single crystal X-ray diffraction.