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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71823생성일: 2026년 10월 23일

Triethylamine → Pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromonaphthalen-1-yl)-2-oxo-ethyl]ester 1-tert-butyl ester

https://huagongshe.com/ko/reaction/71823

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
반응물1-Bromo-4-(bromoacetyl)naphthaleneHCID 59611043—
용매AcetonitrileHCID 6342—
생성물Pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromonaphthalen-1-yl)-2-oxo-ethyl]ester 1-tert-butyl esterHCID 6662017896.2%

반응 단계

Pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (4.85 g) was dissolved in acetonitrile (65 mL), and triethylamine (3.09 mL) was added. A solution of 2-bromo-1-(4-bromonaphthalen-1-yl)-ethanone (6.60 g) in acetonitrile (35 mL) was added. Reaction mixture was stirred 90 minutes and evaporated under vacuum. Oil was dissolved in DCM (50 mL), extracted once with water (20 mL) and once with NaHCO3 solution (20 mL), and evaporated under vacuum to a concentrated liquid. Solution was purified by chromatography (0-50% ethyl acetate:hexane) and evaporated under vacuum, giving pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromonaphthalen-1-yl)-2-oxo-ethyl]ester 1-tert-butyl ester (8.95 g, 95%) as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-84add351f5de42caad8cd1d33f40790b
출처 메모uspto-grants-2014_09