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对羟基苯甲酸 → 3-Methylpentyl p-hydroxybenzoate
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 对羟基苯甲酸 | HCID 135 | — |
| 反应物 | 四氧化硫 | HCID 1118 | — |
| 反应物 | (S)-(+)-3-甲基-戊醇 | HCID 641003 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 产物 | 3-Methylpentyl p-hydroxybenzoate | HCID 19018323 | 80.7% |
反应步骤
13.7 g of p-hydroxybenzoic acid and 11.4 g of (S)-(+)-3-methyl-1-pentanol were refluxed for 10 hours in toluene in the presence of sulfuric acid, while removing out the generated water from the reaction system. Subsequently, the reaction solution was washed with water to remove the sulfuric acid out. The reaction solution was then dried, concentrated, and purified by column chromatography, to obtain 17.8 g of the objective ester compound (liquid state at room temperature ([α]D23 =+7.8° (CHCl3)). (Yield: 80%)
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US05248446 |
| 来源数据集 | uspto-grants-1993_09 |
| ORD ID | ord-9ad13e2b1c894f9687888c893b7a5b06 |
| 来源说明 | uspto-grants-1993_09 |