N,N-Diethylbenzamide → HCID 11287894, compound

Temperature

0 °C

To a solution of N,N-diethylbenzamide (0.18 g, 1.0 mmol) in dry diethylether (5 mL), oxalyl chloride (1.0 mmol, 0.09 mL) was added. The mixture was stirred at 0° C. for one hour under an argon atmosphere. Moreover, the reaction mixture was stirred for three hours at room temperature. The mixture was added to the solution of LiAlHSeH (1.2 mmol), prepared as described above in Example One. The reaction mixture was stirred at room temperature for three hours. The mixture was extracted with diethyl ether and washed with water. The organic layer was dried over sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica gel with dichloromethane to give 0.16 grams (68%) of N,N-diethylbenzselenoamide as a yellow crystal; mp 53–54° C.; C11H15NSe; 1H NMR (CDCl3) δ 1.15 (3H, t, J=6.8 Hz, CH3), 1.45 (3H, t, J=6.8 Hz, CH3), 3.43 (2H, q, J=6.8 Hz, CH2), 4.25 (2H, q, J=6.8 Hz, CH2), 7.21 (2H, d, J=7.6 Hz, Ar), 7.28 (1H, d, J=6.8 Hz, Ar), 7.33 (2H, t, J=7.2 Hz, Ar); 13C NMR (CDCl3) δ 11.2, 13.2, 48.3, 49.7, 123.7, 127.8, 128.0, 146.5, 204.0; 77Se NMR (CDCl3) δ 705.3; MS (CI): m/z=242 [M++1]; HRMS: m/z=241.0369 calcd for C11H15NSe, found 241.0368.

1. stirringMoreover, the reaction mixture was stirred for three hours at room temperature
2. customprepared
3. stirringThe reaction mixture was stirred at room temperature for three hours
4. extractionThe mixture was extracted with diethyl ether
5. washwashed with water
6. dry with materialThe organic layer was dried over sodium sulfate
7. customevaporated to dryness
8. customThe residue was purified by flash chromatography on silica gel with dichloromethane

ORD record

ord-a50f506c0a5f434d8f828a1465574b9a

Source dataset

uspto-grants-2006_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07033564B2