Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 643998생성일: 2026년 10월 26일
p-Fluorophenethylamine → 4-[2-(4-Fluoro-phenyl)-ethylcarbamoyl]-benzenesulfonyl chloride
https://huagongshe.com/reaction/643998
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Fluorophenethylamine | HCID 4653 | — |
| 반응물 | 4-(Chlorosulphonyl)benzoyl chloride | HCID 82024 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-[2-(4-Fluoro-phenyl)-ethylcarbamoyl]-benzenesulfonyl chloride | HCID 86609820 | — |
반응 단계
TEA (474 μL, 3.4 mmol), is added dropwise to a suspension of the title A compound, 4-chlorosulfonyl-benzoyl chloride in DCM (10 mL) at −78° C. To this mixture is added p-fluorophenethylamine over 5 min. After another 10 min at −78° C., the solution is allowed to warm to 0° C. and stirring is continued at this temperature for 1 h. The reaction is quenched by adding it to ice-water (30 mL), and the mixture is extracted with DCM (3×10 mL). The combined organic phases are dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to obtain the crude product which is chromatographed on silica gel using EtOAc as the eluent to give 4-[2-(4-fluoro-phenyl)-ethylcarbamoyl]-benzenesulfonyl chloride.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07700637B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-dd90f2032a8d4d06b81842de02cda08b |
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| 출처 메모 | uspto-grants-2010_04 |
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