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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361054Generated: November 1, 2026

Ammonium Chloride → (S)-3-(2-(4-Fluoro-3-methylphenoxy)acetyl)-4-isopropyloxazolidin-2-one

https://huagongshe.com/reaction/1361054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(4S)-4-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 7157133—
Reactant2-(4-Fluoro-3-methylphenoxy)acetyl chlorideHCID 59775204—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-(2-(4-Fluoro-3-methylphenoxy)acetyl)-4-isopropyloxazolidin-2-oneHCID 59775170—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To the solution of (S)-( )-4-Isopropyl-2-oxazolidinone (992 mg, 5.6 mmol) in anhydrous 30 mL THF at −70° C. was slowly added n-BuLi (3.5 mL, 5.6 mmol, 1.6 M in hexane) over 15 minutes. The reaction mixture was stirred for 30 min at −70° C. and to it was slowly added a solution of 2-(4-fluoro-3-methylphenoxy)acetyl chloride crude solution in 4 mL THF. The resulting mixture was stirred at −70° C. for 2 h and the temperature was slowly raised over a period of 1 h. The mixture was poured into 30 mL saturated NH4Cl and extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine (2×30 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the product isolated by Flash column chromatography eluting with 0% to 50% ethyl acetate/hexane to give 2.2 g of the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879911B2
Source datasetuspto-grants-2011_02
ORD IDord-6b6ae7314e0244298e77f214b3caf32b
Source noteuspto-grants-2011_02