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HRID 67821作成日:2026年10月26日
Oxalyl chloride → cis-3-(2-Chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarbonyl chloride
https://huagongshe.com/reaction/67821
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | cis-3-(2-Chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylic acid | HCID 54318404 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | cis-3-(2-Chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarbonyl chloride | HCID 86737382 | 78.5% |
反応手順
A stirred solution of 10.0 g (0.04 mole) of cis-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylic acid in 100 ml of toluene was heated to 80° C. To this solution at 80° C. was added dropwise over 10 minutes a solution of 10.5 g (0.08 mole) of oxalyl chloride in 5 ml of toluene, and the whole heated at 80° C. for 26 hours. The toluene and excess oxalyl chloride were removed by distillation to give a residual oil which was distilled under reduced pressure using a Kugelrohr distilling system to give 8.2 g of cis-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarbonyl chloride; b.p. 85° C./0.09 mm. The nmr and ir spectra were consistent with the proposed structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04346251 |
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| 出典データセット | uspto-grants-1982_08 |
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| ORD ID | ord-b26f2d1ffb0e4067a5ee0fd96e483e36 |
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| 出典メモ | uspto-grants-1982_08 |
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