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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355211Generated: October 25, 2026

Oxygen → 4-Acetylthio-2-azetidinone

https://huagongshe.com/reaction/355211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactant4-Acetoxy-2-azetidinoneHCID 119981—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418634HCID 178418634—
SolventWaterHCID 962—
Product4-Acetylthio-2-azetidinoneHCID 13132058—

Reaction Steps

To a cold (0°-5°) oxygen-free 1N NaOH solution (803 ml.) was added over 20 minutes thioacetic acid (57 ml., 61 g., 0.803 mole). The resulting solution was added in ca 20 minutes to a cold (10°) oxygen-free solution of 4-acetoxyazetidinone (94 g., 0.730 mole) in water (300 ml.). The pH of the resulting solution was immediately adjusted to 7.4 with solid NaHCO3. The cooling bath was removed and the solution was stirred for 2.75 hours. The mixture was then extracted with chloroform, the combined organic extracts washed with water (150 ml.) and dried over sodium sulfate. Concentration on a rotary evaporator left a yellow oil (95.3 g., 90%) which solidified to a yellow solid on cooling and seeding. This solid was found identical (by IR, NMR and TLC) to the product obtained in Preparation 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04378314
Source datasetuspto-grants-1983_03
ORD IDord-0c3f6067f62543f78a0d0762f06ad3fe
Source noteuspto-grants-1983_03