関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbon Tetrachloride | HCID 5943 | — |
| 反応物 | Benzoyl Peroxide | HCID 7187 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 2-Methyl-5-(2,2,2-trifluoroethoxy)pyridine | HCID 23568433 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Pyridine, 2-(bromomethyl)-5-(2,2,2-trifluoroethoxy)- | HCID 57655951 | 13% |
反応手順
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%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08022062B2 |
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| 出典データセット | uspto-grants-2011_09 |
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| ORD ID | ord-e1def4c742d748bc8e65026f28389864 |
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| 出典メモ | uspto-grants-2011_09 |
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