돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2384534생성일: 2026년 10월 25일

Methyl iodide → (2S,4S)-4-methoxypyrrolidine-2-carboxylic acid

https://huagongshe.com/reaction/2384534

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688414—
반응물HCID 178418361HCID 178418361—
촉매Palladium hydroxideHCID 9942167—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(2S,4S)-4-methoxypyrrolidine-2-carboxylic acidHCID 1284945291%

반응 단계

A stirred solution of (2S,4S)-1-(benzyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid (35.9 g, 135.4 mmol) in dry THF (870 mL) is treated under nitrogen with sodium hydride (11.78 g, 491 mmol) and methyl iodide (38.5 g, 271 mmol), using a procedure similar to that published in J. Med. Chem. 1988, 31, 875, except that reflux is carried out for 16 h. The crude extracted product of this alkylation reaction, (2S,4S)-1-(benzyloxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid, is then dissolved in methanol (200 mL), treated with 6.2 g of 20% palladium hydroxide on carbon, and stirred at room temperature overnight under 1 atmosphere of hydrogen. The reaction mixture is filtered, washed with methanol, and evaporated in vacuo. The resulting solid is suspended in dichloromethane (450 mL) and filtered to give 11.5 g (91%) of the pure title compound: MS: 146 (M+H)+; 500 MHz 1H NMR (d6-DMSO) δ

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08263765B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-eee55e018b0f4237874ecfe1a39fb2f0
출처 메모uspto-grants-2012_09