참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile | HCID 59115159 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile | HCID 54441994 | 77.2% |
반응 단계
5 g (22 mmol) of (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are dissolved in 50 ml of THF and cooled in an ice bath. After adding 4.6 ml (33 mmol) of triethylamine to the solution, 1.9 ml (24 mmol) of methanesulfonyl chloride are added dropwise, keeping the temperature below 5° C. The reaction mixture is stirred while cooling in an ice bath for 30 min. The reaction mixture is poured into 200 ml of water, and extracted with ethyl acetate. The organic phase is washed with hydrochloric acid solution and sodium chloride solution. The organic phase is dried over MgSO4, the solvent is distilled off, and the residue is purified by recrystallization from toluene. 5.2 g (77%) of (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are obtained in the form of greenish brown crystals having a melting point of 160-162° C. (dec.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06004724 |
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| 출처 데이터셋 | uspto-grants-1999_12 |
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| ORD ID | ord-607654a676584d24bb1028defa5a2427 |
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| 출처 메모 | uspto-grants-1999_12 |
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