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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682938Generated: November 2, 2026

4-Methylmorpholine → 1-(3,4,5-Trimethoxybenzoyl)-3-(3,4-dichlorophenyl)-3-(2-hydroxyethyl)pyrrolidine

https://huagongshe.com/reaction/1682938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
Reactant2-(3-(3,4-Dichlorophenyl)pyrrolidin-3-yl)ethanolHCID 18464427—
SolventDichloromethaneHCID 6344—
Product1-(3,4,5-Trimethoxybenzoyl)-3-(3,4-dichlorophenyl)-3-(2-hydroxyethyl)pyrrolidineHCID 1846441771%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(3,4-Dichloro-phenyl)-3-(2-hydroxy-ethyl)-pyrrolidine (288 mg, 1.1 mmol) was dissolved in dichloromethane at -78° C. and treated with 4-methylmorpholine (0.25 mL, 2.27 mmol, 2 eq.) and 3,4,5-trimethoxy-benzoyl chloride (250 mg, 1.1 mmol, 1 eq) in dichloromethane (3 mL). The solution was allowed to warm to 0° C. and stir for 1 hour. 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 353 mg (71%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635510
Source datasetuspto-grants-1997_06
ORD IDord-a44d13ce77594fc6aa6487fd55c8abc5
Source noteuspto-grants-1997_06