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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ozone | HCID 24823 | — |
| Reactant | benzhydryl 2-(benzothiazol-2-yldithio)-alpha-(isopropenyl)-4-oxo-3-[(phenoxyacetyl)amino]azetidine-1-acetate | HCID 99988 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[4-(Benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxo-azetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04301278 |
|---|
| Source dataset | uspto-grants-1981_11 |
|---|
| ORD ID | ord-821e47478d8549b5b7d84681c59c61ae |
|---|
| Source note | uspto-grants-1981_11 |
|---|