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HRID 1033034생성일: 2026년 10월 26일

Propiolic Acid → 2-cyano-3-hydroxy-N-(4-trifluoromethylphenyl)-penta-2,4-dienamide

https://huagongshe.com/reaction/1033034

반응식

참여 물질

역할이름HCID투입량
반응물Propiolic AcidHCID 10110—
반응물Sodium hydrideHCID 24758—
반응물Benzoyl fluorideHCID 67999—
반응물2-Cyano-N-[4-(trifluoromethyl)phenyl]acetamideHCID 3823803—
반응물Prop-2-ynoyl FluorideHCID 5325488—
용매TetrahydrofuranHCID 8028—
생성물2-cyano-3-hydroxy-N-(4-trifluoromethylphenyl)-penta-2,4-dienamideHCID 76178836—

반응 단계

5.0 g (0.22 mole) of 4'-trifluoromethyl-cyanoacetanilide in 150 ml of dry tetrahydrofuran were stirred at room temperature under nitrogen and treated with 2.0 g (0.066 mole) of sodium hydride 80% oil dispersion. The suspension was stirred for 1 hour at room temperature and then was cooled to -70° C. The flask was equipped with an acetone/dry ice condenser and used as the collecting flask from a distillation apparatus charged with 3.01 ml (0.05 mole) of propiolic acid and 15 g of benzoyl fluoride (0.12 mole), as described in J.A.C.S. (1974), Vol. 96 (18), p. 5855 to 5859. The distillation flask was heated in an oil bath at 50° C. and the liberated propynoyl fluoride passed via an air condenser directly into the cold solution of the carbanion. The mixture was stirred at -70° C. for 1 hour and was then quenched by pouring onto a mixture of dilute hydrochloric acid/ice. The mixture was extracted with ethyl acetate and the extracts were dried over magnesium sulfate. The solvent was removed under reduced pressure and triuration with diethyl ether gave colorless crystals of the title compound. Chromatography of the mother liquors over silica gel, eluting with dichloromethane isolated 2.49 g (40%) of the remainder of the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05308865
출처 데이터셋uspto-grants-1994_05
ORD IDord-9bbe61f145674200b72dd14535b0919e
출처 메모uspto-grants-1994_05