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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051097Generated: October 30, 2026

Ethyl chloroformate → HCID 19832672, compound

https://huagongshe.com/reaction/2051097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 19832698HCID 19832698—
SolventPyridineHCID 1049—
ProductHCID 19832672HCID 19832672—

Reaction Conditions

Temperature0 °C

Reaction Steps

55.6 g of N-methoxy-N-methyl-5-amino-2-chloro-4-fluorobenzamide are dissolved in 200 ml of pyridine and the solution is cooled to 0° C. 30.4 g of ethyl chloroformate are added dropwise at 0° C. while stirring and thereafter the reaction mixture is stirred for 14 hours. The mixture is poured into 1 liter of ice-water, the aqueous mixture is extracted three times with 250 ml of ethyl acetate each time, the combined organic phases are washed to neutrality, dried over anhydrous sodium sulphate and the solvent is evaporated off. The product is crystallized from diethyl ether. In this manner there is obtained ethyl 4-chloro-2-fluoro-5-(N-methoxy-N-methylcarbamoyl)-carbanilate, m.p. 121° C., used as the starting material in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017211
Source datasetuspto-grants-1991_05
ORD IDord-41428142b5884442b205a3ac97572918
Source noteuspto-grants-1991_05