Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387193Generated: October 30, 2026

Methyl Acrylate → Methyl (2E)-3-(3-fluoro-2-((((2-methoxy-5-(trifluoromethyl)phenyl)amino)carbonyl)amino)phenyl)-2-propenoate

https://huagongshe.com/reaction/387193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantFuming sulfuric acidHCID 24681—
ReactantN-(2-fluorophenyl)-N'-[2-methoxy-5-(trifluoromethyl)phenyl]ureaHCID 57857532—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
ProductMethyl (2E)-3-(3-fluoro-2-((((2-methoxy-5-(trifluoromethyl)phenyl)amino)carbonyl)amino)phenyl)-2-propenoateHCID 5785753174.4%

Reaction Steps

N-(2-Fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea (0.225 kg) is dissolved in acetic acid (6.75 l) and treated with palladium acetate (30.3 g). 65% strength oleum (247.5 g) is then metered in and methyl acrylate (90 g) is subsequently added. The solution is stirred at room temperature overnight. Subsequently, acetic acid (3740 g) is distilled off at 30° C. and ca. 30 mbar. The suspension is treated with water (2.25 l) and stirred for ca. 1 hour. The product is filtered off with suction, washed twice with water (0.5 l) and dried at 50° C. overnight in the vacuum drying oven using entraining nitrogen. A total of 210.3 g of methyl (2E)-3-{3-fluoro-2-[({[2-methoxy-5-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenyl}acrylate are obtained as a solid, corresponding to 72.2% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372972B2
Source datasetuspto-grants-2013_02
ORD IDord-91f76e224aa14d338eb4d24bf8625b55
Source noteuspto-grants-2013_02