참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | [3-(3-Chloro-phenoxy)-4-methoxy-phenyl]-methanol | HCID 57701122 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Bromomethyl-2-(3-chloro-phenoxy)-1-methoxy-benzene | HCID 57701130 | 91.6% |
반응 단계
To a solution of 3-(3-chloro-phenoxy)-4-methoxy-phenyl]-methanol (13) (315 mg, 1.2 mmol) and triphenylphosphine (390 mg, 1.5 mmol) in methylene chloride (5 ml) was added NBS (0.250 mg, 1.4 mmol) in portions at 0° C. under nitrogen. After 10 min of stirring at 0° C., the mixture was allowed to warm to room temperature, and continued to stir for 16 h. After the solvent was removed, the residue was purified by silica gel column chromatography with ether/hexane as eluent to give 360 mg (85% yield) of product (14).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877816B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-8c044c98209c4847b1ab1c78200d10ff |
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| 출처 메모 | uspto-grants-2014_11 |
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