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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348428Generated: October 25, 2026

Toluene → 4-(Cyclopropylcarbonyl)-alpha,alpha-dimethylbenzeneacetonitrile

https://huagongshe.com/reaction/348428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
Reactant4-CyclopropylcarbonylphenylacetonitrileHCID 15512831—
ReactantPotassium butoxideHCID 23699084—
Product4-(Cyclopropylcarbonyl)-alpha,alpha-dimethylbenzeneacetonitrileHCID 23499845—

Reaction Conditions

Temperature-10 °C

Reaction Steps

4-(Cyclopropylcarbonyl)phenylacetonitrile, 15.5 g [JOC, 1973,16, 487] and methyl iodide, 15.5 ml, are dissolved in 75 ml THF. The mixture is cooled to −10° C. and a solution of potassium butoxide (24.5 g) in THF (75 ml) is added so that the temperature of the reaction is kept below 5° C. After 0.5 h more, HPLC shows the reaction to be complete. 200 ml 2M HCI is added followed by 200 ml toluene. The organics are washed with 100 ml 10%. sodium sulphite solution then 100 ml satd sodium chloride solution. The THF is removed and the toluene treated with 5 g silica to remove colour. The toluene is removed and the product crystallises. Yield, 19 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176318B2
Source datasetuspto-grants-2007_02
ORD IDord-393840dc2e754777826692e274af5201
Source noteuspto-grants-2007_02