HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900473Generated: October 31, 2026
Dicyclohexylcarbodiimide → 2-(2-Cyclopropylacetyl)-5,5-dimethylcyclohexane-1,3-dione
https://huagongshe.com/reaction/900473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1,2-Cyclohexanedione | HCID 13006 | — |
| Reactant | Dimedone | HCID 31358 | — |
| Reactant | Cyclopropaneacetic acid | HCID 138440 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Cyclopropylacetyl)-5,5-dimethylcyclohexane-1,3-dione | HCID 44190459 | 92% |
Reaction Steps
5,5-Dimethyl-1,3-cyclohexanedione (1.051 g, 7.5 mmol, 1.5 eq), cyclopropylacetic acid (500.6 mg, 5.0 mmol), and 4-dimethylaminopyridine (916.3 mg, 7.5 mmol, 1.5 eq) were dissolved in 10 mL of CH2Cl2, cooled to 0° C. in an ice bath. A solution of N,N′-dicyclohexylcarbodiimide (1.238 g, 16.0 mmol, 1.2 eq) in 5 mL of CH2Cl2 was added dropwise over two minutes to the cyclohexanedione solution. The reaction mixture was then stirred at 0° C. for 10 minutes and at room temperature for 16 hours. The reaction mixture was then filtered and the filtrate purified by column chromatography (hexane to 30% EtOAc/hexane) to yield 1.022 g (92% yield) 2-(2-Cyclopropylacetyl)-5,5-dimethyl-cyclohexane-1,3-dione as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358370B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-249c3f304ab640b0985595b53cffba8a |
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| Source note | uspto-grants-2008_04 |
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