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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9667Generated: October 26, 2026

Methanesulfonic Acid → 2-(4-Methoxy-3-methylphenyl)-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethanone

https://huagongshe.com/reaction/9667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant4-Methoxy-3-methylphenylacetic acidHCID 138276—
ReactantSodium BicarbonateHCID 516892—
ReactantThiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-HCID 21986373—
SolventWaterHCID 962—
Product2-(4-Methoxy-3-methylphenyl)-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethanoneHCID 21986370—

Reaction Conditions

Temperature60 °C

Reaction Steps

To methanesulfonic acid (8 ml) in a flask under N2 was added P2O5 (0.56 g), the resulting suspension was heated to 60° C. until a clear solution formed. The mixture was cooled to room temperature prior to addition of 4-methoxy-3-methyl-phenylacetic acid (0.3549) and 4-methyl-2-[4-(trifluoromethyl)phenyl]thiophene (intermediate 102, 0.4 g). The mixture was then heated to 60° C. for 90 minutes. The reaction mixture was cooled to room temperature and then poured into iced water. The suspension was made basic by cautious addition of NaHCO3 and the products extracted into ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and evaporated to yield a brown oil. Purification by flash column chromatography eluting with 5% EtOAc/cyclohexane yielded the title compound as a brown gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-450d571946b54fa997b752c94963e482
Source noteuspto-grants-2006_08