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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54874Generated: October 25, 2026

Water → 3-(4-Butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone

https://huagongshe.com/reaction/54874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(4-Methoxyphenyl)oxiraneHCID 98048—
ReactantLithium ChlorideHCID 433294—
Reactant4-Butylphenyl isocyanateHCID 2796313—
SolventDimethylformamideHCID 6228—
Product3-(4-Butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinoneHCID 1995670214.5%

Reaction Steps

In a 20 ml-three necked flask, 0.013 g of lithium chloride and 3.8 ml of DMF were placed. To the mixture, a solution of 1.09 g (6.22 mM) of 4-butylphenyl isocyanate and 6.20 mM of optically active 4-methoxystyrene oxide in 1.3 ml of DMF was added dropwise in 12 minutes under refluxing and stirring in nitrogen atmosphere, followed by refluxing for 50 minutes under stirring. After the reaction, the reaction mixture was left standing for cooling, then poured into water, and subjected to extraction with ethyl acetate. The organic layer was washed with water, dried with anhydrous sodium sulfate and evaporated under reduced pressure to obtain a residue The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=10/1) and recrystallized from methanol to obtain 0.29 g of optically active 3-(4-butylphenyl)-5-(4-methoxyphenyl)-2-oxazolidinone (Yield: 14.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624600
Source datasetuspto-grants-1997_04
ORD IDord-911e781ae40e4f81bc059adeb5bc3892
Source noteuspto-grants-1997_04