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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252084생성일: 2026년 10월 26일

2,4-Dichlorobenzaldehyde → (S)-tert-Butyl 3-((2,4-dichlorobenzyl)amino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/252084

반응식

참여 물질

역할이름HCID투입량
반응물2,4-DichlorobenzaldehydeHCID 13404—
반응물tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물(S)-tert-Butyl 3-((2,4-dichlorobenzyl)amino)pyrrolidine-1-carboxylateHCID 66854615—

반응 단계

Stir a mixture of (S)-3-amino-pyrrolidine-1-carboxylic acid tert-butyl ester (15.07 g, 81.0 mmol) and 2,4-dichlorobenzaldehyde (13.46 g, 76.9 mmol) in dry methanol (250 mL) at room temperature under nitrogen overnight. Add slowly sodium borohydride (4.74 g, 125.4 mmol) and stir for 10 min. Concentrate and add 2 N NaOH (150 mL) and extract with diethyl ether. Combine the organic layers, wash with saturated aqueous sodium chloride, dry (magnesium sulfate) and concentrate to give (S)-3-(2,4-dichlorobenzylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester which may be used without further purification (26.9 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868014B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-4d67d823c64943d4a40ecc1545da463a
출처 메모uspto-grants-2011_01