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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 457919생성일: 2026년 10월 25일

proline dl-form → 1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/457919

반응식

참여 물질

역할이름HCID투입량
반응물proline dl-formHCID 614—
반응물MethanolHCID 887—
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물(2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acidHCID 58714586—
용매TolueneHCID 1140—
생성물1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylateHCID 58585478—

반응 단계

A solution of the oximether- and/or olefin-type 2-pyrrolidinecarboxylic acid intermediate, e.g. (2S,4EZ)-1-(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid (0.648 g, 2.5 mmol), in a 1:1 mixture of methanol and toluene (35 ml) was made. Trimethylsilyl diazomethane (3.8 ml of a 2M solution in hexanes, 7.5 mmol) was then added dropwise to the stirred solution at room temperature under nitrogen. After completion of the evolution of nitrogen gas, the resulting yellow solution was evaporated in vacuo, and the residue filtered through a pad of silica gel, eluting with ethyl acetate. Removal of solvent from the filtrate gave the methylester product, e.g. 1-tert-butyl 2-methyl(2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate, as a yellow oil (0.646 g, 95% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189754B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-d1b970716bbc4b3c94fe462585b988e2
출처 메모uspto-grants-2007_03