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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645300생성일: 2026년 10월 25일

Sodium Acetate → 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-2-methylbenzoic acid

https://huagongshe.com/reaction/645300

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물1-(4-Bromo-3-methylphenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-oneHCID 76563582—
반응물HCID 178418416HCID 178418416—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-2-methylbenzoic acidHCID 6673524458.2%

반응 단계

To a solution of 4.85 g of 1-(4-bromo-3-methylphenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butene-1-one representing mixed geometrical isomers (isomeric ratio of 8:1) that was synthesized according to Synthetic Examples 1 and 2 and 1.36 g of sodium acetate in 20 mL of 1,2-dimethoxyethane and 20 mL of water in an autoclave, 0.25 g of 1,1′-bis(diphenylphosphino) ferrocene and 50 mg of palladium(II) acetate were added, the mixture was stirred for 5.5 hours at 110° C. in an atmosphere of carbon monoxide at 1.0 MPa. After that, the temperature was cooled to room temperature to isolate solid matter by filtration, diluted hydrochloric acid was added to extract with ethyl acetate, and then an organic layer was dehydrated and dried with saturated saline followed by anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified using silica gel column chromatography that was eluted with ethyl acetate-hexane (1:5) followed by crystallization from a mixed solvent of hexane and a small amount of ethyl acetate to obtain 2.6 g of aimed product as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700808B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-262b3406d7ca4117b24ce37c49d15fc9
출처 메모uspto-grants-2010_04