HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012371Generated: October 26, 2026
Tributylamine → 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride
https://huagongshe.com/reaction/1012371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylamine | HCID 7622 | — |
| 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 | Heptane | HCID 8900 | — |
| Product | 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride | HCID 10657125 | 92.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977509B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f29c107bb3724170b2098ec812571004 |
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| Source note | uspto-grants-2011_07 |
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