参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 二甲基亚砜 | HCID 679 | — |
| 反应物 | 三乙胺 | HCID 8471 | — |
| 反应物 | 草酰氯 | HCID 65578 | — |
| 反应物 | (2-氯吡啶-4-基)甲醇 | HCID 7062237 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 溶剂 | 二氯甲烷 | HCID 6344 | — |
| 产物 | 2-氯吡啶-4-甲醛 | HCID 2762994 | — |
反应步骤
To a solution of oxalyl chloride (42.2 ml) in methylene chloride (1100 ml) is added dropwise a solution of dimethyl sulfoxide (68.7 ml) in methylene chloride (220 ml) at −60° C. to −50° C., and thereto is further added dropwise a solution of 2-chloro-4-hydroxymethylpyridine (63.2 g) in methylene chloride (440 ml) at the same temperature. The mixture is stirred for 15 minutes, and thereto is added dropwise triethylamine (306.6 ml) at the same temperature. The mixture is stirred for five minutes, and warmed to room temperature. After the reaction is complete, to the reaction mixture is added water (2.2 liters). The methylene chloride layer is separated, and the aqueous layer is extracted again with methylene chloride (2.2 liters). The methylene chloride layers are combined, and washed with a saturated aqueous sodium hydrogen carbonate solution, dried, and concentrated under reduced pressure to remove the solvent to give 2-chloropyridine-4-carbaldehyde.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US06214996B1 |
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| 来源数据集 | uspto-grants-2001_04 |
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| ORD ID | ord-c17bac9bc2394de596d47eb8aefdcd61 |
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| 来源说明 | uspto-grants-2001_04 |
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