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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626906Generated: October 25, 2026

Hydrochloric Acid → Methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate

https://huagongshe.com/reaction/626906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactantp-tolylmethyl N-(pyrazine-2-carbonylamino)carbamateHCID 478568—
Reactant4-Methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrileHCID 57468709—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventSodium CarbonateHCID 10340—
ProductMethyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylateHCID 9001507694%

Reaction Conditions

Temperature80 °C

Reaction Steps

Concentrated aq. hydrochloric acid (42 mL, 491.4 mmol) was added to a stirred suspension of 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile [CAS: 951232-17-0] (8.3 g, 31.53 mmol) in methanol (248 mL). The stirred mixture was heated at block temperature of 80° C. for 20 h. The reaction mixture was cooled to ambient temperature, diluted with DCM (500 ml) and Na2CO3 solid was added with stirring. Water (500 ml) was added and the mixture transferred to a separating funnel and shaken (aqueous phase had pH10). The aq. phase was re-extracted with DCM (200 ml) and the combined organic layers were dried (Na2SO4) and evaporated to an oil which solidified, to give 7.6 g after drying. This was dissolved in DCM (30 ml) and the solution was applied to a 340 g silica cartridge which was then eluted on a Biotage SP4 system with a gradient of EtOAc/iso-hexane from 0-75% to give methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate (D29) (6.1 g, approximately 94% pure, contaminated with decarboxylated material);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309254B2
Source datasetuspto-grants-2016_04
ORD IDord-5af05b864aa940ceaa4065926d01a251
Source noteuspto-grants-2016_04