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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1,2-CyclohexanedioneHCID 13006—
ReactantDimedoneHCID 31358—
ReactantCyclopropaneacetic acidHCID 138440—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(2-Cyclopropylacetyl)-5,5-dimethylcyclohexane-1,3-dioneHCID 4419045992%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358370B2
Source datasetuspto-grants-2008_04
ORD IDord-249c3f304ab640b0985595b53cffba8a
Source noteuspto-grants-2008_04