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HRID 2371785作成日:2026年10月25日

Triethylamine → 2-(4-Chlorophenyl)-ethin-1-yl 2,2-difluoro-1-methyl-cycloprop-1-yl ketone

https://huagongshe.com/reaction/2371785

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzene, 1-chloro-4-ethynyl-HCID 70118—
反応物2,2-Difluoro-1-methylcyclopropane-1-carbonyl chlorideHCID 14695232—
触媒copper(I) bromideHCID 24593—
溶媒TolueneHCID 1140—
生成物2-(4-Chlorophenyl)-ethin-1-yl 2,2-difluoro-1-methyl-cycloprop-1-yl ketoneHCID 1469524633%

反応手順

13.7 g (0.1% mol) of p-chlorophenyl-acetylene are added to a mixture of 10.1 g (0.1 mol) of triethylamine, 1.4 g (0.01 mol) of copper(I) bromide and 55 ml of toluene, and the mixture is stirred for 30 minutes at room temperature under argon. After the reaction mixture has been heated to 55° C., 15.5 g (0.1 mol) of 1-methyl-2,2-difluoro-cyclopropanecarbonyl chloride are added dropwise. After this, the mixture is stirred for 8 hours at 90° C., and then cooled and filtered. The filtrate is washed in succession with dilute aqueous hydrochloric acid and water and concentrated under reduced pressure. 19.2 g of a dark oil remain, which is distilled using a bulb tube. At 0.1 mbar and a jacket temperature of 120° C., a yellow oil passes over which solidifies on standing. 8.4 g (33% of theory) of 2-(4-chlorophenyl)-ethin-1-yl 2,2-difluoro-1-methylcycloprop-1-yl ketone of melting point 67°-68° C. are obtained. ##STR65##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05095147
出典データセットuspto-grants-1992_03
ORD IDord-fab03f94dd1b4684a0fb8746bfff9d2c
出典メモuspto-grants-1992_03