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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 645299Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/645299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
Edukt1-(4-Bromophenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-oneHCID 86626427—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acidHCID 66735658—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07700808B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-f060f149bc974205932adc4af2078553
Quellennotizuspto-grants-2010_04