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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901979Generated: October 26, 2026

Water → 2-{(2R)-2-(3,4-dichlorophenyl)-4-[3,5-bis(trifluoromethyl)benzoyl]morpholin-2-yl}ethanol

https://huagongshe.com/reaction/901979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
Reactant(2R)-2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanolHCID 10956756—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-{(2R)-2-(3,4-dichlorophenyl)-4-[3,5-bis(trifluoromethyl)benzoyl]morpholin-2-yl}ethanolHCID 8659979154.2%

Reaction Steps

5.60 g (20.3 mmol) of 2-[(2R)-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol (specification of U.S. Pat. No. 6,159,967, EXAMPLE 51(d)) was dissolved in methylene chloride (60 mL) and 2.83 mL (24.3 mmol) of triethylamine was added thereto. 5.60 g (20.3 mmol) of 3,5-bis(trifluoromethyl)benzoyl chloride and 248 mg (2.03 mmol) of 4-dimethylaminopyridine were added to the mixture under ice-cooling and the mixture was stirred at room temperature for 2 hours under a nitrogen atmosphere. Water was added to the reaction mixture and the methylene chloride layer was washed with water and a saturated NaCl solution and dried over anhydrous magnesium sulfate. After filtration, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (eluting solvent: hexane/ethyl acetate=1/1) to obtain 5.68 g (yield: 54%) of 2-{(2R)-2-(3,4-dichlorophenyl)-4-[3,5-bis(trifluoromethyl)benzoyl]morpholin-2-yl}ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365067B2
Source datasetuspto-grants-2008_04
ORD IDord-b517331a31bc4e709448db23dc9e809a
Source noteuspto-grants-2008_04