Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30901생성일: 2026년 10월 23일
4-Bromo-2-fluoroaniline → N-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amine
https://huagongshe.com/ko/reaction/30901
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-Bromo-2-fluoroaniline | HCID 123050 | — |
| 반응물 | 2-Chloro-6-(trifluoromethoxy)-1,3-benzothiazole | HCID 10037924 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | N-(4-bromo-2-fluorophenyl)-N-(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amine | HCID 21985778 | 58.1% |
반응 단계
In a 250-mL round-bottom flask, 2-chloro-6-trifluoromethoxy-1,3-benzothiazole (5.36 g, 21.14 mmol) and 4-bromo-2-fluoroaniline (4.82 g, 25.36 mmol) were combined in 100 mL n-butanol containing 1% 4.0 M HCl in dioxane, and heated at 90° C. overnight. The mixture was cooled to rt and the solvent was removed under reduced pressure. Ethyl acetate (50 mL) was added, and the mixture was ultrasonicated by suspending the flask in an ultrasonication bath for 30 minutes. The mixture was filtered, and the filtrate was concentrated under reduced pressure. Acetonitrile (50 mL) was added to the mixture, which was then ultrasonicated for 30 minutes and then filtered to provide the product as a white solid (5 g, 58%). LC-MS m/z 409.1 (MH+), ret. time 4.02 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423156B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-90ba5aab8e7741e6b17339b8382e4634 |
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| 출처 메모 | uspto-grants-2008_09 |
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