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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13749Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxylic acidHCID 7413—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(2-Ethyl-butyl)-cyclohexanecarboxylic acidHCID 10488751—
Reactant1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydrideHCID 86612338—
SolventTriethylamineHCID 8471—
Product1-(2-Ethylbutyl)cyclohexanecarbonyl chlorideHCID 1065712592.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728171B2
Source datasetuspto-grants-2010_06
ORD IDord-9bf578c6b1f84623915e90ff2db45623
Source noteuspto-grants-2010_06