戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 64978作成日:2026年10月24日

Hydrochloric Acid → 2,2-Dichlorovinyl 2,4-dichloro-5-fluorophenyl ketone

https://huagongshe.com/ja/reaction/64978

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Vinylidene chlorideHCID 6366—
反応物2,4-Dichloro-5-fluorobenzoyl chlorideHCID 2736821—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒DichloromethaneHCID 6344—
生成物2,2-Dichlorovinyl 2,4-dichloro-5-fluorophenyl ketoneHCID 1364500696.7%

反応手順

136.5 g (0.6 mole) of 2,4-dichloro-5-fluorobenzoyl chloride and 97 g (1 mole) of 1,1-dichloroethylene are successively added dropwise to a suspension of 84 g of anhydrous aluminum chloride in 300 ml of methylene chloride, while cooling with ice and stirring, during which the temperature should not exceed 30° C. The mixture is stirred at room temperature for 3 hours and poured onto a mixture of about 600 g of ice and 60 ml of concentrated hydrochloric acid, the organic phase is separated off and the aqueous phase is subsequently extracted three times with 100 ml of methylene chloride. The methylene chloride solution is washed with 100 ml of water and dried with sodium sulphate and the solvent is distilled off in vacuo. The residue (218.8 g) is heated at 130°-140° C. with 0.34 g of triphenylphosphine until the initially vigorous evolution of HCl has ended (about 3/4 hour). Distillation under a fine vacuum gives 167.1 g (96.4%) of 2,2-dichlorovinyl 2,4-dichloro-5-fluorophenyl ketone of boiling point 121°-123° C./0.13 mbar, melting point 64°-65° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04611080
出典データセットuspto-grants-1986_09
ORD IDord-03763ae0925344f3812ce949ad967c38
出典メモuspto-grants-1986_09