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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974372Generated: October 27, 2026

Hydrochloric Acid → N-(5-allyloxy-4-chloro-2-fluorophenyl)-2-ethoxycarbonyl cyclohexyl carboxylic amide

https://huagongshe.com/reaction/974372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(Ethoxycarbonyl)cyclohexane-1-carboxylic acidHCID 86577—
Reactant5-Allyloxy-4-chloro-2-fluoroanilineHCID 13272926—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-(5-allyloxy-4-chloro-2-fluorophenyl)-2-ethoxycarbonyl cyclohexyl carboxylic amideHCID 14517279—

Reaction Steps

In 20 ml of methylene chloride, 1.20 g of 1,2,3,4,5,6-hexahydrophthalic acid monoethyl ester was dissolved. To this solution 0.47 g of pyridine and 0.71 g of thionyl chloride were added and the resulting mixture was stirred at room temperature. Two hour later, 1 20 g of 5-allyloxy-4-chloro-2-fluoroaniline and 0.61 g of triethylamine were added and the resulting mixture was stirred at room temperature for 5 hours. After completion of the reaction, 10% hydrochloric acid was added to the reaction mixture to make the same acidic and was extracted twice with methylene chloride. The extract was washed with saturated aqueous sodium hydrogen carbonate and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate =5/1 (v/v)) to obtain 1.5 g of light brown crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068365
Source datasetuspto-grants-1991_11
ORD IDord-b4793f4dcc694ffaaa8716244c6ab6e2
Source noteuspto-grants-1991_11