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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723790Generated: October 31, 2026

Acetoxyacetyl chloride → HCID 69365792, compound

https://huagongshe.com/reaction/723790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69364600HCID 69364600—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 69365792HCID 6936579293.1%

Reaction Steps

A solution of (5R)-3-(4-(1,2,5,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one hydrochloride (650 mg, 1.64 mM) in acetone (20 ml) and water (10 ml), was treated with sodium bicarbonate (1.38 g, 16.4 mM) and the mixture cooled to 0–4°. Acetoxyacetyl chloride (448 mg, 3.28 mM) was added dropwise and the reaction mixture stirred at 0–4° for 20 minutes before allowing to warm to ambient temperature. After dilution with water the mixture was extracted well with ethyl acetate. The organic phase was separated, dried (sodium sulfate), solvent evaporated, and the residue triturated with diethyl ether to give the desired product (702 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141583B2
Source datasetuspto-grants-2006_11
ORD IDord-aa85adb0c4804dae94be6b3e8b24d7c0
Source noteuspto-grants-2006_11