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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476921Generated: October 26, 2026

1,3-Dichloro-2-propanol → 5-(Chloromethyl)-3-methyl-2-oxazolidinone

https://huagongshe.com/reaction/476921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-2-propanolHCID 7289—
ReactantMethyl IsocyanateHCID 12228—
ReactantPotassium HydroxideHCID 14797—
CatalystTriethylamineHCID 8471—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-3-methyl-2-oxazolidinoneHCID 1288992567.5%

Reaction Steps

A solution of 64.5 g (0.5 mole) of 1,3-dichloro-2-propanol in 200 ml of methylene chloride was treated with 28.5 g (0.5 mole) of methyl isocyanate and a few drops of triethylamine and allowed to stir at ambient temperature overnight. The solution was concentrated and the residue was dissolved in 200 ml of 95% ethanol and treated with a solution of 33.6 g (0.6 mole) of potassium hydroxide in 300 ml of 95% ethanol. The mixture was stirred at ambient temperature for 3.5 hr and then concentrated. The residue was partitioned between 250 ml of benzene and 100 ml of water. The organic layer was washed successively with 50 ml of a 2N hydrochloric acid solution and 100 ml of brine, dried over anhydrous sodium sulfate and concentrated to give 50.5 g of oil as residue. The oil was subjected to vacuum distillation to yield 36.9 g (49%) of clear oil, b.p. 131°-133° C. at 0.3 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886794
Source datasetuspto-grants-1989_12
ORD IDord-f2c3c2959f044060b5672ffb13c16fb6
Source noteuspto-grants-1989_12