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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647901생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/647901

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Sodium HydroxideHCID 14798—
반응물Ethyl 5-(2-formyl-3-hydroxyphenoxy)pentanoateHCID 9838209—
반응물Sodium thiocresolateHCID 86739085—
용매BenzeneHCID 241—
생성물5-(2-Formyl-3-hydroxyphenoxy)pentanoic acidHCID 72162—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04410537
출처 데이터셋uspto-grants-1983_10
ORD IDord-261005c37ffd402fb2238eacd4b34f05
출처 메모uspto-grants-1983_10