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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329136Generated: October 26, 2026

Boron trifluoride etherate → 2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone

https://huagongshe.com/reaction/329136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-Hydroxy-N-methylacetamideHCID 223579—
Reactant2-(4-Chloro-2-methylphenoxy)acetaldehydeHCID 12391459—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinoneHCID 1239149311%

Reaction Steps

4.6 g (0.0325 mole) of boron trifluoride etherate was added to a solution containing 4.6 g (0.025 mole) of (4-chloro-2-methylphenoxy)acetaldehyde and 2.5 g (0.028 mole) of N-methylglycolamide in 40 ml of tetrahydrofuran. After 24 hours at ambient temperature, the reaction mixture was concentrated under reduced pressure, extracted with ether, washed with water and dried. Purification by silica chromatography gave 0.7 g of 2-(4-chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04019892
Source datasetuspto-grants-1977_04
ORD IDord-703f1d0d6dc940a5b9d2de894fbbb5c3
Source noteuspto-grants-1977_04