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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742431Generated: October 26, 2026

Hydrochloric Acid → methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate

https://huagongshe.com/reaction/742431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopentyl 4-methylbenzene-1-sulfonateHCID 317685—
Reactantmethyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamateHCID 19042327—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
Productmethyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamateHCID 1576684593.1%

Reaction Steps

Methyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamate (1.64 Kg, 7.47 mol), cyclopentyl-p-toluenesulfonate (1.80 Kg, 7.48 mol), potassium carbonate (1.03 Kg, 7.46 mol) and potassium iodide (12.3 g, 1.0 mol %) were placed in a 10L three-necked flask equipped with a stirrer and a Dimroth funnel, and, after adding acetone (7.5 liters) as a solvent thereto, the mixture was refluxed under heating for4 hours. After completion of the reaction, the reaction solution was taken out, and 0.5N hydrochloric acid (20 liters) was added thereto while vigorously stirring. The precipitated methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate as a white solid (2.0 Kg, 6.95 mol, 93.1% yield) was isolated by filtration and thoroughly dired.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554581
Source datasetuspto-grants-1996_09
ORD IDord-2a4e3ab8cf6c471282fa64238545f162
Source noteuspto-grants-1996_09