戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 645299作成日:2026年10月26日

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

https://huagongshe.com/reaction/645299

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物1-(4-Bromophenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-oneHCID 86626427—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
溶媒1,4-DioxaneHCID 31275—
生成物4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acidHCID 66735658—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700808B2
出典データセットuspto-grants-2010_04
ORD IDord-f060f149bc974205932adc4af2078553
出典メモuspto-grants-2010_04