Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178448101 | HCID 178448101 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178448094 | HCID 178448094 | 98% |
Reaction Steps
Toluene (1,000 ml) was added to trans-4-propylcyclohexanecarboxylic acid (1) (500.0 g) in a reaction vessel under an atmosphere of nitrogen, and the mixture was heated to 50° C. Pyridine (0.70 ml) and thionyl chloride (360.0 g) were then added, and the stirring was continued for 3 hours. The unreacted thionyl chloride and the toluene were distilled off at atmospheric pressure. The residue was distilled under reduced pressure (83° C., 3 mmHg) to give trans-4-propylcyclohexanecarboxylic acid chloride (2) (531.7 g) in 98% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389073B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-f105b3a34ccc416292640079d722cd07 |
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| Source note | uspto-grants-2013_03 |
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