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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2090339생성일: 2026년 10월 25일

Ammonia → 4-Bromo-alpha-methylbenzeneethanamine

https://huagongshe.com/reaction/2090339

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1-(4-Bromophenyl)propan-2-oneHCID 736332—
반응물Sodium borohydrideHCID 4311764—
촉매Titanium isopropoxideHCID 11026—
용매EthanolHCID 702—
생성물4-Bromo-alpha-methylbenzeneethanamineHCID 205668—

반응 단계

To a mixture of 2.0 M of ammonia in ethanol (117 mL, 235 mmol, Aldrich, Cat. No. 392685) and titanium tetraisopropoxide (27.7 mL, 93.9 mmol, Aldrich, Cat. No. 377996) was added 1-(4-bromophenyl)acetone (10.0 g, 46.9 mmol, Alfa Aesar, Cat. No. A19028). The reaction mixture was stirred at r.t. under nitrogen overnight. Sodium tetrahydroborate (2.66 g, 70.4 mmol) was added. The mixture was stirred at r.t. for additional 3 h. The reaction mixture was quenched with 2M ammonia in water, and filtered. The solid was washed with AcOEt. The filtrate was concentrated to remove most ethanol, and then was washed with AcOEt twice. The combined organic layers were extracted with 1N HCl aqueous solution (twice). The aqueous HCl solutions were combined, and adjusted with ammonia aqueous solution to pH=10. The result solution was extracted with CH2Cl2. The organic layer was dried with MgSO4, filtered, and concentrated to afford the desired compound which was directly used in the next step reaction without further purification. LCMS (M+H)+: m/z=214.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436008B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-b1413a4f29a04d0095a49d9847b92f74
출처 메모uspto-grants-2013_05