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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732374생성일: 2026년 10월 25일

Ammonium Chloride → 2-(R)-(2-(S)-Dibenzylamino-1-(S)-hydroxy-3-phenylpropyl)-5,5-dimethylpyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/732374

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물SparteineHCID 644020—
반응물(alphaS)-alpha-[Bis(phenylmethyl)amino]benzenepropanalHCID 9883943—
반응물tert-Butyl 2,2-dimethylpyrrolidine-1-carboxylateHCID 57366408—
반응물CID 53628100HCID 178418400—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물2-(R)-(2-(S)-Dibenzylamino-1-(S)-hydroxy-3-phenylpropyl)-5,5-dimethylpyrrolidine-1-carboxylic acid tert-butyl esterHCID 6881524312%

반응 단계

Add sec-butyllithium (2.9 mL, 2.1 mmol) dropwise to a solution of freshly distilled (−)-sparteine (1 mL, 4.3 mmol) in diethyl ether (25 mL) over 3 min at −78° C. Add 2,2-dimethylpyrrolidine-1-carboxylic acid tert-butyl ester (645 mg, 3.2 mmol) in diethyl ether (2 mL) dropwise over 10 min. Stir 2 h, add 2-(S)-dibenzylamino-3-phenylpropionaldehyde (967 mg, 2.9 mmol) in diethyl ether (2 mL) over 5 min and stir 20 min. Add saturated aqueous ammonium chloride solution and ethyl acetate and let warm to room temperature, separate the layers, extract the aqueous layer with ethyl acetate, wash the organic layer with saturated aqueous sodium chloride solution, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 4:1 hexanes:ethyl acetate) to give the title compound as a colorless oil (182 mg, 12%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585885B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-786c264887874d0a88f77749394f9582
출처 메모uspto-grants-2009_09