HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710232Generated: October 30, 2026
HCID 23035687, compound → HCID 23035765, compound
https://huagongshe.com/reaction/1710232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23035687 | HCID 23035687 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23035765 | HCID 23035765 | — |
Reaction Steps
A solution of 0.76 g (10 mmole) of thioacetic acid in 10 ml of 1N sodium hydroxide solution is added dropwise to a solution of 2.19 g (10 mmole) of 4-acetoxy-3-benzylazetidin-2-one (racemic mixture of cis- and trans-isomer in the ratio of 9:13) in 10 ml of dioxan at room temperature under a nitrogen atmosphere, and the mixture is stirred at the same temperature for 3 hours. The reaction mixture is exhaustively extracted with methylene chloride. The combined organic phases are dried over sodium sulphate and concentrated bv evaporation in vacuo. The residue is chromatogra.ohed over silica gel with toluene/ethyl acetate (9:1) and yields a cis-trans mixture of the title compound in the ratio of 2:10. By recrystallisation from methylene chloride/hexane at -10° the pure trans-compound having a melting point of 42°-43° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04952690 |
|---|
| Source dataset | uspto-grants-1990_08 |
|---|
| ORD ID | ord-b984acd7768344398a3b4f3fb38882d8 |
|---|
| Source note | uspto-grants-1990_08 |
|---|