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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 661512생성일: 2026년 10월 27일

Butyl iodide → 2-Butyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester

https://huagongshe.com/reaction/661512

반응식

참여 물질

역할이름HCID투입량
반응물Butyl iodideHCID 10962—
반응물1-Tert-butyl 2-methyl pyrrolidine-1,2-dicarboxylateHCID 394147—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물2-Butyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 6668721869%

반응 조건

온도-78 °C

반응 단계

To a stirred solution of pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (3.00 g, 13.1 mmol) in THF (50 mL) at −78° C. and under nitrogen was added LHMDS (14.4 mL of 1.0 M solution in THF, 14.4 mmol) dropwise. After 30 minutes, a solution of 1-iodobutane (2.23 mL, 19.7 mmol) in THF (1 mL) was added dropwise. The reaction mixture was stirred for 30 minutes at −78° C., warmed to ambient temperature over 90 minutes, then quenched by the addition of saturated aqueous NH4Cl and extracted with EtOAc. The combined extracts were washed with saturated aqueous NaHCO3 and brine then dried (MgSO4), filtered and concentrated in vacuo to a yellow oil (4.5 g). Purification by chromatography (silica, 10% EtOAc in hexanes) gave 2-butyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (2.57 g, 9.01 mmol, 69%) as a clear colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084623B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-eff591d2f427453ebf38d31f7e602612
출처 메모uspto-grants-2011_12