Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377106Generated: October 26, 2026

Potassium Iodide → 5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-one

https://huagongshe.com/reaction/1377106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl ChlorideHCID 6327—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Methyl-5-(4-chlorobenzylidene)-cyclopentanoneHCID 53752951—
Solventtert-ButanolHCID 6386—
Product5-[(4-Chlorophenyl)methylidene]-2,2-dimethylcyclopentan-1-oneHCID 53421021100.1%

Reaction Steps

106 g of 2-methyl-5-(4-chlorobenzylidene)-cyclopentanone, 49.5 g of 85% strength aqueous potassium hydroxide solution, 8.3 g of potassium iodide and 400 g of tert-butanol were weighed in succession into a 700 ml stainless steel autoclave, and 50.5 g of methyl chloride were injected at 20° C. The mixture was stirred at room temperature for 23 hours and then 300 ml of tert-butanol were distilled off at 20 mbar up to an overhead temperature of max. 50° C. 400 ml of water were added to the residue, and the mixture was stirred thoroughly. The resulting suspension was filtered off over a suction filter, and the filter cake was washed twice with 200 ml of water each time and dried. 112.8 g of a pale beige solid were thus obtained with a purity of 89.5%. The yield of the crude product was 90.2% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663447
Source datasetuspto-grants-1997_09
ORD IDord-81f1c423030e48d895584eec98bf4d1e
Source noteuspto-grants-1997_09