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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Butyl iodide | HCID 10962 | — |
| 반응물 | 1-Tert-butyl 2-methyl pyrrolidine-1,2-dicarboxylate | HCID 394147 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Butyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester | HCID 66687218 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08084623B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-eff591d2f427453ebf38d31f7e602612 |
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| 출처 메모 | uspto-grants-2011_12 |
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