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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1181396생성일: 2026년 10월 27일

Carbamate → Benzenemethanamine, N-methyl-4-(trifluoromethyl)-

https://huagongshe.com/reaction/1181396

반응식

참여 물질

역할이름HCID투입량
반응물CarbamateHCID 276—
반응물Ammonium ChlorideHCID 25517—
반응물4-(Trifluoromethyl)benzylamineHCID 76804—
반응물Carbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
반응물Aluminium lithium hydrideHCID 21226445—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물Benzenemethanamine, N-methyl-4-(trifluoromethyl)-HCID 485420—

반응 단계

A mixture of 4-(trifluoromethyl)benzylamine (1.0 mL, 7.02 mmol) and di-tert-butyl carbonate (1.68 g, 7.72 mmol) in CH2Cl2 (10 mL) was stirred for 1 hour. The reaction mixture was poured into saturated aqueous ammonium chloride solution, extracted with CH2Cl2 and the organic layers were combined, dried over MgSO4 and concentrated in vacuo to give a white crystalline solid. To a solution of the crude carbamate (1.00 g, 3.61 mmol) in THF (20 mL) in a room temperature water bath, was added LiAlH4 (0.69 g, 18.1 mmol) portion-wise over 10 minutes. The reaction was then heated at reflux for 4 hours. The reaction was cooled in ice and quenched by the addition of water (1.6 mL) and NaOH (2N, 1.3 mL). The grey slurry was filtered and washed with MeOH. The MeOH was removed in vacuo and the crude product taken up in CH2Cl2 and dried over MgSO4 and concentrated in vacuo. Purification by flash column chromatography eluting with 5-10% MeOH in CH2Cl2 plus 1% NH3 solution (2N in MeOH) afforded the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07285563B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-0fd7b82f0ea3401aac99be59d275d7d7
출처 메모uspto-grants-2007_10