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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155441Generated: October 29, 2026

Ozone → 2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxo-azetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester

https://huagongshe.com/reaction/1155441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactantbenzhydryl 2-(benzothiazol-2-yldithio)-alpha-(isopropenyl)-4-oxo-3-[(phenoxyacetyl)amino]azetidine-1-acetateHCID 99988—
SolventEthyl AcetateHCID 8857—
Product2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxo-azetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl esterHCID 86736448—

Reaction Steps

1 equivalent of ozone (diluted with oxygen) is passed into a solution, cooled to -70° C., of 681 mg (1.0 mM) of 2-[4-(benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid diphenylmethyl ester in 30 ml of ethyl acetate. The reaction solution is allowed to warm up, concentrated to 10 ml in vacuo, mixed with 1.0 ml of dimethyl sulphide and stirred for 15 hours at room temperature. Solvent and excess reagent are removed in vacuo and the residue is chromatographed on 30 g of acid-washed silica gel, using toluene/ethyl acetate, 4:1 (15 ml fractions). 2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester is obtained as a solid amorphous substance. [α]D =130°±1° (CHCl3 ; c=0.8) IR spectrum (CH2Cl2): 2.95, 5.60, 5.92, 6.04 and 8.10μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04301278
Source datasetuspto-grants-1981_11
ORD IDord-821e47478d8549b5b7d84681c59c61ae
Source noteuspto-grants-1981_11