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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764342Generated: October 25, 2026

Phosgene → 5-{[(6-Methylpyridin-3-yl)oxy]methyl}-3-(propan-2-yl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1764342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant1-[(6-Methylpyridin-3-yl)oxy]-3-[(propan-2-yl)amino]propan-2-olHCID 20483467—
SolventTolueneHCID 1140—
Solvent2,6-LutidineHCID 7937—
Solvent1,4-DioxaneHCID 31275—
Product5-{[(6-Methylpyridin-3-yl)oxy]methyl}-3-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 20483445—

Reaction Steps

A solution of 10 g of phosgene in 40 ml of toluene is added dropwise at 5°-10° C. to 15.6 g of 3-(2'-hydroxy-3'-isopropylamino-propoxy)-6-methyl-pyridine, dissolved in 75 ml of dioxane, in the presence of 8 ml of 2,6-lutidine, whilst stirring. The reaction mixture is stirred overnight at room temperature and is then evaporated in vacuo. The evaporation residue is rendered alkaline with a little concentrated sodium hydroxide solution and is extracted with 200 ml of ethyl acetate. The organic phase is evaporated, initially at approx. 20 mm Hg and then at 0.01 mm Hg/60° C. bath temperature. Approx. 50 ml of ether are added to the residue which remains, giving crystalline 3-isopropyl-5-[(6-methylpyridin-3-yloxy)methyl]-oxazolidin-2-one of melting point 86°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115575
Source datasetuspto-grants-1978_09
ORD IDord-12e687f3a59c4b90a4ef8f5c73bfeeb7
Source noteuspto-grants-1978_09