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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722984Generated: October 27, 2026

Pyridine → ethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamate

https://huagongshe.com/reaction/1722984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantBenzenamine, 4-chloro-2-fluoro-5-(1-methylethoxy)-HCID 158649—
SolventDichloromethaneHCID 6344—
Productethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamateHCID 20026143—

Reaction Steps

12.8 g of ethyl chloroformate are added while stirring to a solution of 20 g of 4-chloro-2-fluoro-5-isopropoxyaniline in 100 ml of methylene chloride at room temperature. 9.4 g of pyridine are subsequently added dropwise during 20 minutes at 20° C. while stirring and cooling. The reaction mixture is stirred for 20 minutes, washed three times with in each case 200 ml of a solution of 20 ml of 2N hydrochloric acid in 200 ml of water, dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. There is obtained ethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamate, m.p. 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859229
Source datasetuspto-grants-1989_08
ORD IDord-bd4e217845554cfe96ccae5c5490f16d
Source noteuspto-grants-1989_08