関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-chloropyridine N-oxide | HCID 70724 | — |
| 反応物 | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (4-Chloropyridin-2-yl)methanol | HCID 2763167 | 61.8% |
反応手順
4-chloropyridine-N-oxide (4.4 g) was dissolved in methylene chloride (68 ml), trimethyloxonium tetrafluoroborate (5.0 g) was added to the mixture, and the mixture was stirred for 90 minutes at room temperature. The solvent was removed under reduced pressure, the obtained residue was dissolved in methanol, and an aqueous solution (6.8 ml) of ammonium peroxodisulfate (1.54 g) was added thereto under heat reflux. An aqueous solution (3.4 ml) of ammonium peroxodisulfate (0.77 g) was further added to the mixture after 30 minutes, the mixture was stirred for 1 hour. After allowing the mixture to be cooled to room temperature, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give (4-chloro-2-pyridinyl)methanol (3.0 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07262185B2 |
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| 出典データセット | uspto-grants-2007_08 |
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| ORD ID | ord-fcfad3eb9f514b6b93e4e0d6044f8814 |
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| 出典メモ | uspto-grants-2007_08 |
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