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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280378Generated: October 29, 2026

Hydrochloric Acid → Ethyl [2-{2-chloro-4-fluoro-5-[2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}phenoxy]acetate

https://huagongshe.com/reaction/1280378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-amino-4,4,4-trifluorocrotonateHCID 5702529—
ReactantEthyl [2-(2-chloro-4-fluoro-5-ethoxycarbonylaminophenoxy)phenoxy]acetateHCID 17812347—
SolventDimethylformamideHCID 6228—
ProductEthyl [2-{2-chloro-4-fluoro-5-[2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]phenoxy}phenoxy]acetateHCID 17812334—

Reaction Conditions

Temperature0 °C

Reaction Steps

To ethyl 3-amino-4,4,4-trifluorocrotonate are added N,N-dimethylformamide and sodium hydride and the mixture is stirred at 0° C. Thereafter, to the reaction solution is added a mixture of ethyl [2-(2-chloro-4-fluoro-5-ethoxycarbonylaminophenoxy)phenoxy]acetate [Intermediate compound A8-23] and N,N-dimethylformamide, and the mixture is stirred at 80° C. Then reaction solution is cooled to room temperature, then, poured into a mixture of hydrochloric acid and ice water, and the deposited crystal is collected by filtration to obtain ethyl [2-{2-chloro-5-[2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]-4-fluorophenoxy}phenoxy]acetate.s

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451740B2
Source datasetuspto-grants-2002_09
ORD IDord-bde760c38ec9434aabcb499be798ab45
Source noteuspto-grants-2002_09