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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038048생성일: 2026년 10월 26일

Diisopropylamine → 1-Tert-butyl 3-methyl 3-fluoropyrrolidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1038048

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물N-FluorobenzenesulfonimideHCID 588007—
반응물1-Tert-butyl 3-methyl pyrrolidine-1,3-dicarboxylateHCID 4572775—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Tert-butyl 3-methyl 3-fluoropyrrolidine-1,3-dicarboxylateHCID 5951134664%

반응 단계

n-Butyl lithium (2.5M/Hexanes, 3.83 ml; 9.575 mmol) added dropwise to solution of diisopropylamine (1.36 ml; 9.62 mmol) at −78° C. Solution was allowed warm to room temperature and stirred for 30 minutes, then cooled to −78° C. A solution of Pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester (2 g, 8.72 mmol) in THF (10 ml) was added dropwise, warmed to −40° C. for 1 hour, then cooled to −70° C.A solution of N-fluorobenzene-sulfonimide (3.02 g, 9.57 mmol) in THF (15 ml) was added dropwise, stirred at −78° C. for 1 hour, then stirred at room temperature overnight. Precipitated solid was filtered, washed with EtOAc (2×150 ml). Organic layer was washed with 1N HCl (30 ml), brine (100 ml), dried (MgSO4), filtered and solvent evaporated. The residue was chromatographed on silica gel eluting with 10% v/v EtOAc/hexanes yielding product as colorless oil (1.38 g: 64% yield). MS (ESMS, MH 249).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546404B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-e5331fb5c1804399b654c1dd450ca831
출처 메모uspto-grants-2013_10