참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Tetrachloride | HCID 5943 | — |
| 반응물 | Benzoyl Peroxide | HCID 7187 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | 2-Methyl-5-(2,2,2-trifluoroethoxy)pyridine | HCID 23568433 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Pyridine, 2-(bromomethyl)-5-(2,2,2-trifluoroethoxy)- | HCID 57655951 | 13% |
반응 단계
Add 2-methyl-5-(2,2,2-trifluoroethoxy)-pyridine (2.5 g, 13.1 mmol), NBS (2.3 g, 13.1 mmol) and benzoyl peroxide (50 mg) to a flask containing carbon tetrachloride (30 mL). Heat the mixture at 80° C. in a sealed flask for 16 h. Cool the flask, add NBS (1.1 g, 6.5 mmol) and benzoyl peroxide (100 mg), then continue heating at 80° C. for an additional 5 h. Cool the mixture, dilute with DCM, then wash with saturated sodium bisulfite (10 mL). Collect the organic layer and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (9:1) to obtain the desired intermediate (460 mg, 13%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08022062B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-e1def4c742d748bc8e65026f28389864 |
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| 출처 메모 | uspto-grants-2011_09 |
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