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HRID 234816생성일: 2026년 10월 26일

Hydrochloric Acid → 4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acid

https://huagongshe.com/reaction/234816

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Maleic AnhydrideHCID 7923—
반응물Benzene, 1-chloro-4-fluoro-HCID 9604—
반응물Aluminum(III) ChlorideHCID 6451240—
생성물4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acidHCID 10823270—

반응 단계

Finely pulverized maleic anhydride (3.0 g) is added portionwise to a mixture of 1-chloro-4-fluorobenzene (24.6 g) and anhydrous aluminium chloride (11.56 g). A gas bubbler is attached to the top of the condenser and the mixture is heated in an oil bath at 80°-85° C. for 2 hours at which time little hydrogen chloride gas evolution is evident. The mixture is cooled and the excess 1-chloro-4-fluorobenzene is recovered by distillation at water aspirator pressure. The resultant mixture is quenched with ice and then steam distilled to remove the last traces of the 1-chloro-4-fluorobenzene. Concentrated hydrochloric acid (10 mL) is added to the cooled mixture and the resultant solid collected by filtration (9.2 g). This material is taken up in boiling benzene (50 mL), treated with decolorizing charcoal and filtered through a celite bed. On standing overnight, the yellow solid is collected by filtration (2.45 g). A second recrystallization from benzene (40 mL) leads to 4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acid (2.1 g) as pure regioisomer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596097
출처 데이터셋uspto-grants-1997_01
ORD IDord-ff49ab663d7f4e0ca144a2d5ec31f538
출처 메모uspto-grants-1997_01