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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278184Generated: November 3, 2026

Dimethyl Sulfoxide → 3-Fluoro-2-morpholinobenzaldehyde

https://huagongshe.com/reaction/2278184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DifluorobenzaldehydeHCID 137664—
SolventWaterHCID 962—
Product3-Fluoro-2-morpholinobenzaldehydeHCID 2618875128.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 100 mL round-bottom flask was charged with 2,3-difluorobenzaldehyde (2.00 g, 14.1 mmol, 1.00 equiv), morpholine (1.84 g, 21.1 mmol, 1.50 equiv), potassium carbonate (4.90 g, 35.4 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 (50 mL). The resulting solution was extracted with dichloromethane (3×20 mL) and the organic layers were combined, washed with H2O (3×50 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 (1/20) to yield 0.840 g (28% yield) of 3-fluoro-2-(morpholin-4-yl)benzaldehyde as a yellow solid. 1H NMR 300 MHz, (CDCl3) δ 10.54 (s, 1H), 7.63 (d, J=7.5 Hz, 1H), 7.18-7.34 (m, 2H), 3.85 (br, 4H), 3.23 (br, 4H). LCMS (ESI, m/z): 210 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133148B2
Source datasetuspto-grants-2015_09
ORD IDord-46a2152046994f7cb22b9f71b10585c8
Source noteuspto-grants-2015_09