戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 348818作成日:2026年10月25日

Sodium Cyanide → Ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl)benzoate

https://huagongshe.com/reaction/348818

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CyanideHCID 8929—
反応物Ethyl 3-(bromomethyl)-5-[(dipropylamino)carbonyl]benzoateHCID 21086099—
溶媒Dimethyl SulfoxideHCID 679—
生成物Ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl)benzoateHCID 21086102—

反応手順

A mixture of ethyl 3-[(dipropylamino)carbonyl]-5-(hydroxymethyl)benzoate (1.5 g) and phosphorous tribromide (0.95 mL) is stirred in dichloromethane (10 mL) and heated at 50 degrees C. for 4 hours and then cooled and partitioned between dichloromethane and water. The organic phase is separated and washed with aqueous sodium bicarbonate and then dried over magnesium sulfate and taken to dryness to give ethyl 3-(bromomethyl)-5-[(dipropylamino)carbonyl]benzoate, high resolution MS MH+=370.1020. Ethyl 3-(bromomethyl)-5-[(dipropylamino)carbonyl]benzoate (1.4 g) and sodium cyanide (0.2 g) are stirred in dry DMSO (25 mL) at 20–25 degrees C. for 3.5 hours and the mixture is then partitioned between ethyl acetate, water and saline. The organic layer is separated and dried over magnesium sulfate and taken to dryness under reduced pressure to give ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl]benzoate. Ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl]benzoate (0.6 g) is hydrolyzed with lithium hydroxide monohydrate (0.1 g) in ethanol and water at 20–25 degrees C. overnight and then added to water (50 mL). The pH is adjusted to 4 using concentrated hydrochloric acid and the mixture is partitioned between ethyl acetate, water, and saline. The organic phase is separated and dried over magnesium sulfate and taken to dryness under reduced pressure to give 3-(cyanomethyl)-5-[(dipropylamino)carbonyl]benzoic acid, MS M+H=287.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176242B2
出典データセットuspto-grants-2007_02
ORD IDord-2e14a7470aba42bfb510a8538dbde8ba
出典メモuspto-grants-2007_02