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HRID 13749作成日:2026年10月23日

Cyclohexanecarboxylic acid → 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride

https://huagongshe.com/ja/reaction/13749

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexanecarboxylic acidHCID 7413—
反応物Thionyl ChlorideHCID 24386—
反応物1-(2-Ethyl-butyl)-cyclohexanecarboxylic acidHCID 10488751—
反応物1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydrideHCID 86612338—
溶媒TriethylamineHCID 8471—
生成物1-(2-Ethylbutyl)cyclohexanecarbonyl chlorideHCID 1065712592.9%

反応条件

温度50 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728171B2
出典データセットuspto-grants-2010_06
ORD IDord-9bf578c6b1f84623915e90ff2db45623
出典メモuspto-grants-2010_06