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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | proline dl-form | HCID 614 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 반응물 | (2S,4EZ)-1(tert-butoxycarbonyl)-4-(methoxyimino)-2-pyrrolidinecarboxylic acid | HCID 58714586 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-tert-butyl 2-methyl (2S,4EZ)-4-(methoxyimino)-1,2-pyrrolidinedicarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07189754B2 |
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| 출처 데이터셋 | uspto-grants-2007_03 |
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| ORD ID | ord-d1b970716bbc4b3c94fe462585b988e2 |
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| 출처 메모 | uspto-grants-2007_03 |
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