関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Benzene, 1-chloro-4-ethynyl- | HCID 70118 | — |
| 反応物 | 2,2-Difluoro-1-methylcyclopropane-1-carbonyl chloride | HCID 14695232 | — |
| 触媒 | copper(I) bromide | HCID 24593 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-(4-Chlorophenyl)-ethin-1-yl 2,2-difluoro-1-methyl-cycloprop-1-yl ketone | HCID 14695246 | 33% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05095147 |
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| 出典データセット | uspto-grants-1992_03 |
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| ORD ID | ord-fab03f94dd1b4684a0fb8746bfff9d2c |
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| 出典メモ | uspto-grants-1992_03 |
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