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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058193Generated: November 2, 2026

Pyridine → 4-Acetoxy-3-phenylacetamidoazetidin-2-one

https://huagongshe.com/reaction/2058193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium ThiosulfateHCID 24477—
ReactantPotassium PermanganateHCID 516875—
Reactant4-Acetoxy-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamidoazetidin-2-oneHCID 12907759—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Acetoxy-3-phenylacetamidoazetidin-2-oneHCID 1112910619%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-acetoxy-1-(1-methoxycarbonyl-2-methylprop-1-enyl)-3-phenylacetamidoazetidin-2-one (709 mg, 1.9 mmol [R. J. Stoodley and N. R. Whitehouse, J. Chem. Soc., Perkin I, 32(1973).] in 5 ml dimethylformamide, 5 ml pyridine and 1 ml water at 0° C. in an ice-water bath is added 497 mg (3.15 mmol) solid potassium permanganate. The mixture is stirred at 0° C. under a nitrogen atmosphere for 1.0 hour. The mixture is treated with sufficient aqueous sodium thiosulfate to destroy the excess permanganate and is diluted with ethylacetate. The mixture is filtered and the filtrate is partitioned between ethylacetate and dilute aqueous hydrochloric acid. The organic phase is separated and is washed successively with dilute aqueous sodium bicarbonate and brine. The organic phase is dried (MgSO4), filtered, and evaporated. The residue is purified by plate layer chromatography [1 development φH-EtOAc (1:1)] to give 95.1 mg (19%) of 1; nmr (CDCl3) 2.03, 3H(s); 3.5, 2H(s); 4.67; 1H(dd, J=1 Hz, 7 Hz); 5.73, 1H(d, J=1 Hz); 7.17, 6H(s); 7.53, 1H(bs). ##STR40##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04215124
Source datasetuspto-grants-1980_07
ORD IDord-5e84458e7a35471bb3614f1a3179b399
Source noteuspto-grants-1980_07