関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl Alcohol | HCID 244 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | Oxane-4-carboxylic acid | HCID 219302 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Benzyl tetrahydro-2H-pyran-4-carboxylate | HCID 23131611 | 70.1% |
反応手順
A mixture of tetrahydropyran-4-yl-carboxylic acid (910 mg, 6.99 mmol) and SOCl2 (5.0 mL) was stirred for 1 h at 60° C. and concentrated in vacuo. To the residue were added benzyl alcohol (1.52 g, 14.1 mmol) and tetrahydrofuran (5.0 mL) at ambient temperature. The resulting mixture was stirred for 13 h at ambient temperature and concentrated in vacuo. The residue was purified by preparative thin layer chromatography (silica gel, eluting with hexane/ethyl acetate (2:1)) to give 1.08 g (70%) of the title compound as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07737163B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-8fd06a8b3539453b86ef5bd3c688a452 |
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| 出典メモ | uspto-grants-2010_06 |
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