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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanecarboxylic acid | HCID 7413 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid | HCID 10488751 | — |
| Reactant | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydride | HCID 86612338 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride | HCID 10657125 | 92.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07728171B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-9bf578c6b1f84623915e90ff2db45623 |
|---|
| Source note | uspto-grants-2010_06 |
|---|