Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Azetidon | HCID 10935078 | — |
| Reactant | HCID 178514124 | HCID 178514124 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 9907013 | HCID 9907013 | 90.1% |
Reaction Steps
To a solution of 4-(R)acetoxy-3(R)-[1(R)t-butyldimethylsilyloxyethyl]azetidin-2-one (2.87 g) in dioxane (40 ml) the potassium salt of carbamoyloxythioacetic acid (2.1 g) was added. Zinc bromide (2.7 g) was added to the resulting suspension and the reaction mixture was stirred for 4 hours at 40° C. The reaction mixture was then cooled at room temperature and poured in a mixture of ethyl acetate and water. The organic layer was separated, washed twice with water, dried over anhydrous sodium sulfate, and evaporated in vacuo. The solid residue was taken-up with CH2Cl2. Upon addition of hexanes and cooling a white solid was precipitated, and collected by filtration to give 3.26 g of the title product (90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399679 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-5ea93d28b46e46058a89eebc0f95ef09 |
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| Source note | uspto-grants-1995_03 |
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