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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461285Generated: October 26, 2026

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

https://huagongshe.com/reaction/461285

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 numberUS04062670
Source datasetuspto-grants-1977_12
ORD IDord-8691e936157a42a4bc5f2f957447cd70
Source noteuspto-grants-1977_12