Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269468생성일: 2026년 10월 26일
Pyridine → N-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamide
https://huagongshe.com/reaction/1269468
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | N-[4-cyano-3-(trifluoromethyl)phenyl]-2,3-dihydroxy-2-methylpropanamide | HCID 9882395 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamide | HCID 12148451 | — |
반응 단계
A solution of 46 g (0.16 mol) of N-[4-cyano-3-trifluoromethyl-phenyl]-2,3-dihydroxy-2-methyl-propionamide in 1 1 of dichloromethane and 46 ml (0.57 mol) of dry pyridine was cooled to 0° C. and 46 ml (0.59 mol) of methanesulfonyl chloride was added dropwise. The mixture was stirred at 0° C. for 5 h, then washed three times with 500 ml of saturated aqueous sodium hydrogen carbonate, 500 ml of 10% aqueous hydrochloric acid and 500 ml of brine. The organic layer was dried over sodium sulfate and concentrated in vacuum. The residue was crystallized with 200 ml of petroleum ether, which has a boiling range of 40–70° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07199257B1 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-b35866d175fd4d758effefbba81c681b |
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| 출처 메모 | uspto-grants-2007_04 |
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