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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539615Generated: October 25, 2026

Ethyl chloroacetate → (R)-5-(4-fluoro-phenyl)-morpholin-3-one

https://huagongshe.com/reaction/539615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium hydrideHCID 24758—
Reactant(R)-2-Amino-2-(4-fluorophenyl)ethanolHCID 10583003—
SolventTetrahydrofuranHCID 8028—
Product(R)-5-(4-fluoro-phenyl)-morpholin-3-oneHCID 5820026445.7%

Reaction Steps

To a stirring mixture of NaH (1.1 g, 45.7 mmol) in THF (30 mL) at room temperature under N2 atmosphere was added dropwise a solution of (R)-2-amino-2-(4-fluoro-phenyl)-ethanol (5.0 g, 32.2 mmol) in THF (50 mL). The reaction mixture was stirred at room temperature for 30 minutes, then cooled to 0° C. A solution of ethyl chloroacetate (4.0 g, 33 mmol) in THF (30 mL) was added dropwise, and the reaction mixture was stirred for 30 minutes at 0° C., then stirred at room temperature for two hours. The reaction mixture was concentrated under reduced pressure, and water (50 mL) was added to the residue. The resulting mixture was pH adjusted to approximately 6.5 by addition of 1M aqueous HCl, and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was recrystallized from diethyl ether to give 2.87 g of (R)-5-(4-fluoro-phenyl)-morpholin-3-one. The mother liquor from the recrystallization was concentrated and purified via chromatography (50-70% ethyl acetate in hexanes) to give an additional 1.0 g of (R)-5-(4-fluoro-phenyl)-morpholin-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871760B2
Source datasetuspto-grants-2014_10
ORD IDord-e1c7f7e980c14a3c97dca3877aff3af4
Source noteuspto-grants-2014_10