関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trimethyl orthoformate | HCID 9005 | — |
| 反応物 | Trimethylolmethane | HCID 78432 | — |
| 反応物 | 1,3-Difluoroacetone | HCID 228397 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | (2,2-Bis(fluoromethyl)-1,3-dioxan-5-yl)methanol | HCID 59792580 | 43.4% |
反応手順
A mixture of 2-(hydroxymethyl)-1,3-propanediol (2.2 g, 20.7 mmol), 1,3-difluoroacetone (3.89 g, 41.4 mmol), trimethyl orthoformate (3.44 ml, 20.7 mmol), and p-toluenesulfonic acid monohydrate (356 mg, 2.07 mmol) was stirred at 60° C. for 10 hours. After completion of the reaction, triethylamine (577 μl) was added to the reaction mixture, which was then concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (1.6 g, yield: 43.4%) as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07425634B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-643f1dd86f91404aa5f5e314bc0f49bb |
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| 出典メモ | uspto-grants-2008_09 |
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