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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71832생성일: 2026년 10월 24일

Triethylamine → Pyrrolidine-1,2-dicarboxylic acid 2-[2-(6-bromo-naphthalen-2-yl)-2-oxo-ethyl]ester 1-tert-butyl ester

https://huagongshe.com/ko/reaction/71832

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
반응물2-Bromo-1-(6-bromonaphthalen-2-yl)ethanoneHCID 12698898—
용매AcetonitrileHCID 6342—
생성물Pyrrolidine-1,2-dicarboxylic acid 2-[2-(6-bromo-naphthalen-2-yl)-2-oxo-ethyl]ester 1-tert-butyl esterHCID 6662020684.3%

반응 단계

Pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (24.0 g) was dissolved in acetonitrile (330 mL), and triethylamine (15.6 mL) was added. A solution of 2-bromo-1-(6-bromonaphthalen-2-yl)-ethanone (33.0 g) in acetonitrile (170 mL) were added. Reaction mixture was stirred over 3 days and evaporated under vacuum. Oil was dissolved in dichloromethane (100 mL), extracted with water (50 mL) and with NaHCO3 solution (50 mL), and evaporated under vacuum to a concentrated liquid. Solution was purified by chromatography (0-30% ethyl acetate:hexane) and evaporated under vacuum, giving pyrrolidine-1,2-dicarboxylic acid 2-[2-(6-bromo-naphthalen-2-yl)-2-oxo-ethyl]ester 1-tert-butyl ester (39.2 g, 84%) as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d3afa0d21e7e4d4ea1b935e19af96b2a
출처 메모uspto-grants-2014_09