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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227545Generated: October 26, 2026

Hydrochloric Acid → (2R)-2-[2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl]ethanol

https://huagongshe.com/reaction/227545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
Reactant(2R)-2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanolHCID 10956756—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
Product(2R)-2-[2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl]ethanolHCID 12042117104.5%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a mixture of (2R)-2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol (25 g, 90.3 mmol) and acetonitrile (125 ml), triethylamine (27.4 g, 271 mmol) was added under a nitrogen stream, the resulting mixture was cooled to 0-5° C., then a solution of 3,4,5-trimethoxybenzoyl chloride (21.24 g, 92.1 mmol) in toluene (100 ml) was further added dropwise at below 10° C., and then the mixture was stirred at 0-5° C. for one hour. After completion of the reaction, toluene (150 ml), water (125 ml) and concentrated hydrochloric acid (25 ml) were added to the reaction mixture, and the resulting mixture was partitioned. The separated organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate and water, and concentrated to afford (2R)-2-[2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl]ethanol (44.4 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560549B2
Source datasetuspto-grants-2009_07
ORD IDord-d14ec9bb909849c6aea7a07340e91c86
Source noteuspto-grants-2009_07