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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1350975생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1350975

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물Ethyl 3-(bromomethyl)-5-[(dipropylamino)carbonyl]benzoateHCID 21086099—
용매Dimethyl SulfoxideHCID 679—
생성물Ethyl 3-(cyanomethyl)-5-[(dipropylamino)carbonyl)benzoateHCID 21086102—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07214715B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-540f011c4c1f4e098cd3e6da3c5c6cd7
출처 메모uspto-grants-2007_05