참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-chloropyridine N-oxide | HCID 70724 | — |
| 반응물 | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (4-Chloropyridin-2-yl)methanol | HCID 2763167 | 61.8% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07262185B2 |
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| 출처 데이터셋 | uspto-grants-2007_08 |
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| ORD ID | ord-fcfad3eb9f514b6b93e4e0d6044f8814 |
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| 출처 메모 | uspto-grants-2007_08 |
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