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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012371Generated: October 26, 2026

Tributylamine → 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride

https://huagongshe.com/reaction/1012371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(2-Ethyl-butyl)-cyclohexanecarboxylic acidHCID 10488751—
Reactant1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydrideHCID 86612338—
SolventHeptaneHCID 8900—
Product1-(2-Ethylbutyl)cyclohexanecarbonyl chlorideHCID 1065712592.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 6.0 kg (28.3 mol) 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid and 20.6 mL tributylamine (0.085 mmol) in 10 L heptane was warmed to 50° C. 2.5 L (34.5 mol) of thionyl chloride was added during 40 minutes at a temperature of 40-50° C. (reaction is endothermic, vigorous gas evolution) and the reaction mixture was kept at 53-55° C. An IPC-control after 60 minutes indicated complete conversion (0.04% 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid and no 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid anhydride). After removing volatile components under reduced pressure (70° C. bath, 13-8 mbar) 6.86 kg of the residue was obtained (assay 92.5% 1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride, yield 97.2%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977509B2
Source datasetuspto-grants-2011_07
ORD IDord-f29c107bb3724170b2098ec812571004
Source noteuspto-grants-2011_07