Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278180Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 89676979, compound

https://huagongshe.com/reaction/2278180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-(trifluoromethyl)benzaldehydeHCID 522929—
SolventWaterHCID 962—
ProductHCID 89676979HCID 8967697941.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 100 mL round-bottom flask was charged with 2-fluoro-4-(trifluoromethyl)benzaldehyde (1.90 g, 9.89 mmol, 1.00 equiv), morpholine (1.30 g, 14.9 mmol, 1.51 equiv), potassium carbonate (3.45 g, 25.0 mmol, 2.52 equiv), and dimethyl sulfoxide (20 mL). The resulting solution was stirred overnight at 100° C. in an oil bath and diluted with H2O (30 mL). The resulting solution was extracted with dichloromethane (2×20 mL) and the organic layers were combined, washed with H2O (3×20 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on a silica gel column with ethyl acetate/petroleum ether (1/5) to yield 1.06 g (41% yield) of 2-(morpholin-4-yl)-4-(trifluoromethyl)benzaldehyde as yellow oil. LCMS (ESI, m/z): 260 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133148B2
Source datasetuspto-grants-2015_09
ORD IDord-1057620b02424f78862df7e102301ef7
Source noteuspto-grants-2015_09