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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252085생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/252085

반응식

참여 물질

역할이름HCID투입량
반응물2,4-DichlorobenzaldehydeHCID 13404—
반응물tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매DichloromethaneHCID 6344—
생성물(S)-tert-Butyl 3-((2,4-dichlorobenzyl)amino)pyrrolidine-1-carboxylateHCID 6685461546.4%

반응 단계

Alternatively, add sodium triacetoxyborohydride (1.6 g, 7.6 mmol) to a mixture of (S)-3-aminopyrrolidine-1-carboxylic acid tert-butyl ester (1 g, 5.4 mmol) and 2,4-dichlorobenzaldehyde (2.8 g, 16.2 mmol) in 1,2-dichloroethane (10 mL) and stir overnight at room temperature. Dilute with dichloromethane and wash with saturated aqueous sodium chloride, dry (magnesium sulfate) concentrate and chromatograph on silica gel to give (S)-3-(2,4-dichlorobenzylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester (865 mg, 33%). 1H NMR (400 MHz, CDCl3) 7.33-7.38 (2H, m), 7.23 (1H, d, J=7.82 Hz), 3.85 (2H, d, J=1.96 Hz), 3.45-3.56 (2H, m), 3.30-3.40 (2H, m), 3.19-3.10 (1H, m), 2.04 (1H, m), 1.74 (1H, m), 1.46 (9H, s), MS (ES): m/z=345 [M+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868014B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-fe6f6a67c45741deb82c820dec456437
출처 메모uspto-grants-2011_01