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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592293생성일: 2026년 10월 26일

Chlorotrimethylsilane → Tert-butyl 3-(benzylamino)-3-phenylpropanoate

https://huagongshe.com/reaction/1592293

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Tert-butyl cinnamateHCID 347555—
반응물N-BenzyltrimethylsilylamineHCID 519016—
반응물(1R,2R)-1,2-dimethoxy-1,2-diphenylethaneHCID 10988459—
반응물ButyllithiumHCID 178418339—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물Tert-butyl 3-(benzylamino)-3-phenylpropanoateHCID 1148375397%

반응 단계

Under an argon atmosphere, n-butyllithium (0.9 mL, 1.6 M in hexane solution, 1.5 mmol) was added to a solution of N-benzyltrimethylsilylamine (0.3 mL, 1.5 mmol) in toluene (4 mL) at −78° C. over 5 min. After stirring for 0.5 hr, a solution of (1R,2R)-1,2-dimethoxy-1,2-diphenylethane (436 mg, 1.8 mmol) in toluene (2 mL) was added, and the mixture was stirred at −78° C. for 0.5 hr. Thereto was added a solution of tert-butyl cinnamate (204 mg, 1.0 mmol) and chlorotrimethylsilane (0.63 mL, 5.0 mmol) in toluene (2 mL) over 5 min. The mixture was stirred at −78° C. for 5 hr, and quenched with saturated aqueous ammonium chloride solution (1.5 mL). After adding a saturated aqueous sodium hydrogen carbonate solution (20 mL), the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over sodium sulfate, after which it was concentrated and subjected to silica gel column chromatography (ethyl acetate/hexane=1/25) to give the title compound (302 mg, yield 97%) as a colorless oil of [α]25D+32.5 (c 1.35, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291752B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-74c45471a807477491462f41d3d46361
출처 메모uspto-grants-2007_11