Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | Cyclohexanecarboxylic acid, 3,5-dioxo-, ethyl ester | HCID 11252382 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13391496 | HCID 13391496 | 45.6% |
Reaction Steps
4.2 g of ethyl 3,5-dioxocyclohexanecarboxylate and 3.4 g of triethylamine were dissolved in 50 ml of dichloromethane, to which was added dropwise 2.9 g of propionyl chloride under stirring at room temperature. The resultant mixture was allowed to react at ambient temperature for 2 hours, after which the reaction solution was washed with water and admixed with a dilute aqueous sodium bicarbonate solution to remove the acidic matters from the reaction solution. The organic layer was then separated from the aqueous phase, dried and concentrated to a small volume. The concentrated solution was taken up in 20 ml of toluene, followed by addition of 0.5 g of 4-N,N-dimethylaminopyridine and heating the mixture at 85° C. for 3 hours. Thereafter, the toluene was removed from the reaction solution by distillation under reduced pressure, and the residue was chromatographed on silica gel using benzene as developing solvent to afford 2.5 g of the title compound (Compound No. 9 of Table 1) as colorless flakes having a melting point of 55°- 56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560403 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-8a7c3c2547e84550bc8bf360a849855f |
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| Source note | uspto-grants-1985_12 |
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