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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279249생성일: 2026년 10월 25일

1-Chloro-4-(chloromethyl)benzene → (R)-tert-Butyl (1-(4-chlorobenzyl)pyrrolidin-3-yl)carbamate

https://huagongshe.com/reaction/279249

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참여 물질

역할이름HCID투입량
반응물1-Chloro-4-(chloromethyl)benzeneHCID 7723—
반응물N,N-DipropylethylamineHCID 519799—
반응물tert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
용매DimethylformamideHCID 6228—
생성물(R)-tert-Butyl (1-(4-chlorobenzyl)pyrrolidin-3-yl)carbamateHCID 1842622480.2%

반응 조건

온도70 °C

반응 단계

4-Chlorobenzyl chloride (4.15g, 25.8 mmol) and Pr2NEt (6.67 g, 51.6 mmol) were added to a solution of 3-{(tert-butoxycarbonyl)amino)pyrrolidine (4.81 g, 25.8 mmol) in DMF (50 mL}. The reaction mixture was stirred at 70° C. for 15 h and the solvent was removed under reduced pressure. Recrystallization (CH3CN, 50 mL) provided the desired material, 3-(tert-butoxycarbonyl)amino-1-(4-chlorobenzyl)pyrrolidine as a pale yellow solid (6.43 g, 80.2%): 1H NMR (CDCl3, 300 MHz) δ1.37 (s, 9H), 1.5-1.7 (br, 1H), 2.1-2.4 (m, 2H), 2.5-2.7 (m, 2H), 2.83 (br, 1H), 3.57 (s, 2H), 4.1-4.3 (br, 1H), 4.9-5.1 (br, 1H), 7.15-7.35 (br, 4H); The purity was determined by RPLC/MS (98%); ESI/MS m/e 311.0 (M++H, C16H24ClN2O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-a4707587aa2a46fdb2586597e2570602
출처 메모uspto-grants-2002_03