Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 2-(Bromomethyl)-3-chloro-1-benzothiophene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Phosphorus tribromide | HCID 24614 | — |
| 반응물 | (3-Chloro-1-benzothien-2-yl)methanol | HCID 821965 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-(Bromomethyl)-3-chloro-1-benzothiophene | HCID 816708 | — |
반응 단계
To a solution of (3-chloro-1-benzothiophen-2-yl)methanol (480 mg, 2.4 mmol) in anhydrous diethyl ether (8 mL) was added dropwise a solution of phosphorus tribromide (230 μL, 2.4 mmol) in anhydrous diethyl ether (2 mL) at 0° C. The mixture was stirred for 3 hours at room temperature. Water was added and extracted 3 times with ethyl acetate. The combined organic phase was washed with brine and dried over magnesium sulfate. After evaporation of the solvent, 2-(bromomethyl)-3-chloro-1-benzothiophene was obtained as a pink pale solid (537 mg, 85% yield) and used for the next step without further purification; 1H NMR (400 MHz, CDCl3): δ 4.81 (s, 2H), 7.40-7.48 (m, 2H), 7.76-7.82 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09040538B2 |
| 출처 데이터셋 | uspto-grants-2015_05 |
| ORD ID | ord-a02e62eea5164712a3ce5b589e66f62e |
| 출처 메모 | uspto-grants-2015_05 |