戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 647901作成日:2026年10月25日

Hexamethylphosphoramide → 5-(2-Formyl-3-hydroxyphenoxy)pentanoic acid

https://huagongshe.com/reaction/647901

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylphosphoramideHCID 12679—
反応物Sodium HydroxideHCID 14798—
反応物Ethyl 5-(2-formyl-3-hydroxyphenoxy)pentanoateHCID 9838209—
反応物Sodium thiocresolateHCID 86739085—
溶媒BenzeneHCID 241—
生成物5-(2-Formyl-3-hydroxyphenoxy)pentanoic acidHCID 72162—

反応手順

Ethyl 5-(2-formyl-3-methoxphenoxy)pentanoate (Example 4) (2.0 g, 0.00704 M), sodium thiocresolate (2.06 g, 0.014 M), hexamethylphosphoramide (2.48 ml, 0.014 M) and benzene (10 ml) were placed in a round bottom flask and refluxed for 18 hours. The reaction mixture, containing ethyl 5-(2-formyl-3-hydroxyphenoxy)pentanoate, was then cooled and poured into 2 N sodium hydroxide solution (20 ml). The organic layer was removed, diluted with ether (20 ml), then extracted with 2 N sodium hydroxide solution (2×20 ml). The aqueous layers were combined and extracted with dichloromethane (2×20 ml). The organic layer was discarded and the aqueous layer acidified with concentrated hydrochloric acid. The resulting precipitate was filtered, washed with water and dried in a desiccator over phosphorus pentoxide to give 5-(2-formyl-3-hydroxyphenoxy)pentanoic acid, m.p. 98°-99° C. from ethyl acetate/petrol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04410537
出典データセットuspto-grants-1983_10
ORD IDord-261005c37ffd402fb2238eacd4b34f05
出典メモuspto-grants-1983_10