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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12299Generated: October 29, 2026

Methyl iodide → Methyl 2-(4-chlorophenyl)-2-cyclopentylpropanoate

https://huagongshe.com/reaction/12299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantMethyl 2-(4-chlorophenyl)-2-cyclopentylacetateHCID 23092013—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
SolventButyllithiumHCID 178418339—
ProductMethyl 2-(4-chlorophenyl)-2-cyclopentylpropanoateHCID 23092040—

Reaction Conditions

Temperature-35 °C

Reaction Steps

To a solution of diisopropylamine (0.15 ml) in THF (2 ml), n-butyl lithium (1.5 M hexane solution, 0.6 ml) was added at −78° C., stirred for 10 minutes and another solution of methyl 2-(4-chlorophenyl)-2-cyclopentylacetate (200 mg) in THF (1.5 ml) was added dropwise. After 15 minutes' stirring, the system temperature was raised to −35° C., and methyl iodide (0.15 ml) was added. The reaction liquid temperature was raised to 0° C., and the liquid was stirred for 1.5 hours, diluted with saturated aqueous ammonium chloride solution and extracted with diethyl ether. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and condensed under reduced pressure. The resulting residue was purified on silica gel column chromatography (hexane/ethyl acetate 60/1) to provide methyl 2-(4-chlorophenyl)-2-cyclopentylpropionate (180 mg) as yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727998B2
Source datasetuspto-grants-2010_06
ORD IDord-605b849843804862a90b8e36f41a45f4
Source noteuspto-grants-2010_06