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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245329Generated: October 30, 2026

Ammonium Chloride → (S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one

https://huagongshe.com/reaction/245329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCarbamic acid, N-(3-fluoro-4-(4-morpholinyl)phenyl)-, phenylmethyl esterHCID 5306150—
Reactant2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
Reactant(S)-1-chloro-3-(dibenzylamino)propan-2-olHCID 49765557—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-oneHCID 1121366860%

Reaction Conditions

Temperature-30 °C

Reaction Steps

N-carbobenzoxy-3-fluoro-4-morpholinylaniline (0.33 g, 1 mmol) was added to 8 mL of acetone. The solution was cooled to −30° C. under the protection of nitrogen flow and then 50 mmol of lithium tert-butoxide was added. The mixture was stirred at −30° C.˜20° C. for 2 hours, (S)-1-chloro-3-(dibenzylamino)propan-2-ol (2.9 g, 10 mmol) was added and then the solution was heated slowly to 60° C. and stirred for 2 hours. After the solution was cooled down, saturated ammonium chloride solution and ethyl acetate were added to separate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness to provide 285 mg of white solid in 60% yield. HPLC: 99.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658789B2
Source datasetuspto-grants-2014_02
ORD IDord-c2ddfa3bc3884930880b94bc309e891d
Source noteuspto-grants-2014_02