関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyclohexanecarboxylic acid | HCID 7413 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid | HCID 10488751 | — |
| 反応物 | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydride | HCID 86612338 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride | HCID 10657125 | 92.9% |
反応手順
A mixture of 103.0 mmol 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid, 38.9 mmol cyclo-hexanecarboxylic acid and 396 μL triethylamine (2.84 mmol=0.02 eq. relative to the sum of both acids) was warmed to 50° C. 12.4 mL (170.3 mmol=1.2 Eq. relative to the sum of both acids) of thionyl chloride was added during 18 minutes at a temperature of 40-54° C. (reaction is endothermic, vigorous gas evolution) and the reaction mixture was kept at 54-55° C. After 1 hr reaction was complete (0.03% 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid and no 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid anhydride). After removing volatile components in vacuo (60° C. bath, 3.5-4.3 mbar followed by 120° C. bath, 10-11 mbar) 25.44 g of residue was obtained (assay 92.9% 1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride, yield 99.4%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728171B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-9bf578c6b1f84623915e90ff2db45623 |
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| 出典メモ | uspto-grants-2010_06 |
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