Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2405813생성일: 2026년 10월 24일
Methanesulfonyl chloride → 1-Tert-butoxycarbonylamino-2-(2-methanesulfonyloxyethyl)cyclopropanecarboxylic acid methyl ester
https://huagongshe.com/ko/reaction/2405813
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 1-tert-Butoxycarbonylamino-2-(2-hydroxyethyl)-cyclopropanecarboxylic acid methyl ester | HCID 56605397 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Tert-butoxycarbonylamino-2-(2-methanesulfonyloxyethyl)cyclopropanecarboxylic acid methyl ester | HCID 57445167 | 84.5% |
반응 단계
1-tert-Butoxycarbonylamino-2-(2-hydroxyethyl)-cyclopropanecarboxylic acid methyl ester (0.500 g, 1.93 mmol, from Example 104) was diluted in 8 mL DCM and cooled to 0° C. under an Ar atmosphere. TEA (0.54 mL, 3.9 mmol) and methanesulfonyl chloride (0.30 mL, 3.9 mmol) were added sequentially. After 2.5 h, the solvent was removed in vacuo and the residue taken up in EtOAc and H2O (15 mL each). The aqueous layer was extracted with 3×10 mL EtOAc. The combined organics were washed with brine and dried over anhydrous MgSO4. Following concentration in vacuo, the residue was purified by column chromatography on SiO2 (0 to 50% Hex/EA) to produce 1-tert-butoxycarbonylamino-2-(2-methanesulfonyloxyethyl)cyclopropanecarboxylic acid methyl ester (0.55 g, 84%). LCMS found 360.1 [M+Na]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08809267B2 |
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| 출처 데이터셋 | uspto-grants-2014_08 |
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| ORD ID | ord-de5d82ac96ca436caa7c6c2a67f89645 |
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| 출처 메모 | uspto-grants-2014_08 |
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