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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682942Generated: November 3, 2026

4-Methylmorpholine → [3-(3,4-Dichlorophenyl)-3-(2-hydroxyethyl)pyrrolidin-1-yl](2-methoxyphenyl)methanone

https://huagongshe.com/reaction/1682942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
Reactant2-(3-(3,4-Dichlorophenyl)pyrrolidin-3-yl)ethanolHCID 18464427—
SolventDichloromethaneHCID 6344—
Product[3-(3,4-Dichlorophenyl)-3-(2-hydroxyethyl)pyrrolidin-1-yl](2-methoxyphenyl)methanoneHCID 5395380261.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(3,4-Dichloro-phenyl)-3-(2-hydroxy-ethyl)-pyrrolidine, (218 mg, 0.83 mmol) was dissolved in dichloromethane at -78° C. and treated with 4-methylmorpholine (0.19 mL, 1.73 mmol, 2 eq.) and 2-methoxybenzoyl chloride (155 mg, 0.84 mmol, 1 eq.) in dichloromethane (3×1 mL). The solution was allowed to warm to 0° C. and stir for 4.5 hours. The solution was washed with 1N HCl and 5% sodium bicarbonate and the organic phase was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel (30 g) with a gradient of 50% ethyl acetate in hexane to 6% methanol in dichloromethane to give 202 mg (60%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635510
Source datasetuspto-grants-1997_06
ORD IDord-552f059a12ba47afbd1c516499ccffd1
Source noteuspto-grants-1997_06