돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645299생성일: 2026년 10월 24일

Water → 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid

https://huagongshe.com/ko/reaction/645299

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물1-(4-Bromophenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-oneHCID 86626427—
반응물HCID 178418416HCID 178418416—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매1,4-DioxaneHCID 31275—
생성물4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acidHCID 66735658—

반응 단계

To a solution of 1.95 g of 1-(4-bromophenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butene-1-one that was synthesized under Synthetic Example 3 and 0.56 g of triethylamine in 10 mL of tertiary-butyl alcohol, 10 mL of dioxane, and 5 mL of water in an autoclave, 51 mg of 1,1′-bis(diphenylphosphino) ferrocene and 10 mg of palladium(II) acetate were added, the mixture was stirred for 4 hours at 110° C. in an atmosphere of carbon monoxide at 0.5 MPa followed by cooling to room temperature, and then further 10 mg of palladium(II) acetate were added, the mixture was stirred for 4 hours at 110° C. in an atmosphere of carbon monoxide at 0.5 MPa. After that, the temperature was cooled to room temperature to isolate solid matter by filtration whereto diluted hydrochloric acid was added to extract with ethyl acetate, and then an organic layer was dried with anhydrous sodium 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 (1:8) to obtain 1.5 g of aimed product as resinous matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700808B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-f060f149bc974205932adc4af2078553
출처 메모uspto-grants-2010_04