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Triethylamine → 2-((Benzyloxy)methyl)-1,3-dioxane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,3-Propanediol | HCID 10442 | — |
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 生成物 | 2-((Benzyloxy)methyl)-1,3-dioxane | HCID 59792378 | 58% |
反応手順
A mixture of benzyloxyacetaldehyde (3.6 g, 24 mmol), 1,3-propanediol (5.2 ml, 72 mmol), triethyl orthoformate (4 ml, 24 mmol), and p-toluenesulfonic acid monohydrate (414 mg, 2.45 mmol) was stirred at room temperature for 17 hours. To the reaction mixture, triethylamine (669 μl, 4.8 mmol) was added, which was concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (2.9 g, yield: 58%) as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07425634B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-9f39e15806ee44feb5cf00cee9492e0e |
| 出典メモ | uspto-grants-2008_09 |