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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252970Generated: November 2, 2026

p-Toluenesulfonic acid monohydrate → Isopropyl 2-chloro-4-fluoro-5-{3-[2-(methoxycarbonyl)propenyl]ureido}-benzoate

https://huagongshe.com/reaction/1252970

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantMethyl 3-methoxy-2-methyl-acrylateHCID 3019052—
ReactantIsopropyl 2-chloro-4-fluoro-5-ureidobenzoateHCID 20130672—
SolventBenzeneHCID 241—
ProductIsopropyl 2-chloro-4-fluoro-5-{3-[2-(methoxycarbonyl)propenyl]ureido}-benzoateHCID 54564066—

Reaction Steps

27.4 g of isopropyl 2-chloro-4-fluoro-5-ureidobenzoate and 13.0 g of methyl 3-methoxy-2-methyl-acrylate are heated under reflux for 2 hours in 250 ml of benzene with 1.9 g of toluene-4-sulphonic acid monohydrate. The reaction mixture is evaporated to dryness under reduced pressure and the residue is stirred with 400 ml of diethyl ether. The insoluble material is filtered off under suction and the filtrate is evaporated to dryness under reduced pressure. The residue is purified by chromatography on 1 kg of silica gel using ethyl acetate/n-hexane (1:3) as the eluent. There is obtained isopropyl 2-chloro-4-fluoro-5-{3-[2-(methoxycarbonyl)propenyl]ureido}-benzoate, m.p. 189°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04746352
Source datasetuspto-grants-1988_05
ORD IDord-9f6c3169fb534556aaa091a80ef5c8e2
Source noteuspto-grants-1988_05