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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601023Generated: October 25, 2026

Morpholine → Methyl 2-chloro-4-morpholin-4-ylbenzoate

https://huagongshe.com/reaction/601023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-Chloro-4-fluorobenzoateHCID 2763551—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl 2-chloro-4-morpholin-4-ylbenzoateHCID 333027065%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-4-fluoro-benzoic acid methyl ester (3.51 g, 18.6 mmol), morpholine (1.95 mL, 22.3 mmol) and potassium carbonate (5.12 g, 37.1 mmol) in N-methylpyrrolidinone (20 mL) was stirred at 120° C. for 5 h. The reaction was cooled, diluted with ethyl acetate and filtered through Celite. The filtrate was washed four times with water, once with brine, was dried (sodium sulfate) and evaporated. Purification by flash chromatography (SiO2) eluted with 2:8 ethyl acetate:hexanes to provide 2-chloro-4-morpholin-4-yl-benzoic acid methyl ester (3.08 g, 65% yield) as a white solid. 1H-NMR (CDCl3, 500 MHz) 7.79 (d, 1H), 6.81 (d, 1H), 6.67 (dd, 1H), 3.81 (s, 3H), 3.78 (m, 4H), 3.20 (m, 4H) ppm; MS (FIA) 256.1 (M+H); HPLC (Method A) 3.275 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902239B2
Source datasetuspto-grants-2011_03
ORD IDord-fc6db544f4694bd786e5b9bd0cd81dc9
Source noteuspto-grants-2011_03