참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfide | HCID 1068 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Chlorosuccinimide | HCID 31398 | — |
| 반응물 | 2,4,5-Trifluoroaniline | HCID 94953 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 2-Methylthiomethyl-3,4,6-trifluoroaniline | HCID 18974461 | — |
반응 단계
To 2,4,5-trifluoroaniline (35.0 g) are added anhydrous dichloromethane (530 ml) and dimethyl sulfide (24.6 ml) and the mixture is cooled to 0° C. Thereto N-chlorosuccinimide (38.2 g) is gradually added below 5° C. After the mixture is stirred at the same temperature for 15 minutes, triethylamine (47.7 ml) is gradually added. After reflux for 12 hours, the resultant is made alkaline with 5% aqueous sodium hydroxide solution, extracted with dichloromethane, and the extract is dried over sodium sulfate and concentrated. The residue is purified with column chlomatography (silica-gel, dichloromethane: n-hexane=1: 4) to give 2-methylthiomethyl-3,4,6-trifluoroaniline (22.3 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05563138 |
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| 출처 데이터셋 | uspto-grants-1996_10 |
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| ORD ID | ord-c7c8453ffd6a405a93d4bd410e46506d |
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| 출처 메모 | uspto-grants-1996_10 |
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