Hexamethylphosphoramide → Methyl-(1-methyl-4-nitro-4-phenyl-butyl)-carbamic acid tert-butyl ester

関与物質

反応条件

反応手順

To a −78° C. solution of 304 mg (2.219 mmol) nitromethyl-benzene (CAS: 622-42-4) in 5 ml tetrahydrofuran over mol-sieve and 1.29 ml HMPA, was added dropwise 2.91 ml (4.654 mmol) n-BuLi (1.6 M in hexane). After 45 minutes at −78° C., a solution of 590.7 mg (2.219 mmol) (3-bromo-1-methyl-propyl)-methyl-carbamic acid tert-butyl ester in 1.5 ml tetrahydrofuran over mol-sieve was added dropwise. After 1 hour at −78° C., the reaction mixture was allowed to warm up slowly, during 2 hours, to −15° C. The mixture was then cooled again to −78° C. and quenched with 0.75 ml of acetic acid, then with 13 ml saturated ammonium chloride. Back to room temperature, the aqueous phase was extracted two times with ethylacetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on silica (Eluent: heptane/ethyl acetate 0 to 10%) to provide 201 mg (28%) of the title compound as a colorless oil. MS (m/e): 323.3 (M+H).

情報源と証拠