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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70106생성일: 2026년 10월 24일

Methyl iodide → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid

https://huagongshe.com/ko/reaction/70106

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물N-[tert-butoxycarbonyl]-L-serineHCID 98766—
반응물Sodium ethoxideHCID 2723922—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acidHCID 7016354—

반응 단계

Under nitrogen a mixture of 74 ml abs. THF and 6 ml abs. methanol is cooled to −70° C. and 2 g sodium hydride (55-65% dispersion) are added. The suspension is stirred for 0.4 hour at ambient temperature. Under nitrogen, 2.05 g N-Boc-L-serine are suspended in 100 ml abs. THF and 40 ml of the prepared sodium ethoxide solution are added. The suspension is stirred for 1 hour at ambient temperature and 1 ml methyliodide are added. After 1 hour the remainder of the sodium ethoxide solution and another 2 ml of methyliodide are added. After 18 hours the reaction mixture is evaporated to dryness. The residue is washed with water and ether and extracted. The water phase is acidified and extracted with ethyl acetate and dichloromethane. 0.52 g of the product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822474B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1a7854345f3e4da0922298bdc2c9bd38
출처 메모uspto-grants-2014_09