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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248559Generated: October 30, 2026

Acetic Acid → isopropyl 2-chloro-4-fluoro-5-[2-methoxy-6-oxo-4-trifluoromethyl-1(6H)-pyrimidinyl]-benzoate

https://huagongshe.com/reaction/2248559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium MethoxideHCID 10942334—
Reactantisopropyl 2-chloro-5-[2-chloro-6-oxo-4-trifluoromethyl-1(6H)-pyrimidinyl]-4-fluorobenzoateHCID 19994245—
SolventMethanolHCID 887—
Productisopropyl 2-chloro-4-fluoro-5-[2-methoxy-6-oxo-4-trifluoromethyl-1(6H)-pyrimidinyl]-benzoateHCID 19994237—

Reaction Steps

51.3 ml of a 2N solution of sodium methylate in methanol are added dropwise while stirring and cooling at 0° C. during 5 minutes to a solution of 42.4 g of isopropyl 2-chloro-5-[2-chloro-6-oxo-4-trifluoromethyl-1(6H)-pyrimidinyl]-4-fluorobenzoate in 100 ml of absolute methanol. The reaction mixture is stirred at 0° C. for 10 minutes and adjusted to about pH 4 with concentrated acetic acid. Subsequently, the reaction mixture is evaporated to dryness under reduced pressure. The residue is dissolved in 300 ml of diethyl ether and the solution is washed twice with 100 ml of water each time. The organic phase is dried over anhydrous sodium sulphate and evaporated to dryness. The residue is purified by chromatography on a silica gel column using n-hexane/diethyl ether (3:1) as the eluent and is subsequently recrystallized from n-hexane/diethyl ether. There is obtained isopropyl 2-chloro-4-fluoro-5-[2-methoxy-6-oxo-4-trifluoromethyl-1(6H)-pyrimidinyl]-benzoate, m.p. 121°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041156
Source datasetuspto-grants-1991_08
ORD IDord-dcfc5bc49c574c28ba2478ca122be3bf
Source noteuspto-grants-1991_08