HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10086774, compound → cis-3-acetoxy-4-phenylazetidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10086774 | HCID 10086774 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | cis-3-acetoxy-4-phenylazetidin-2-one | HCID 11009062 | — |
Reaction Steps
The above procedure may, in turn, be followed by modification of the lactam formed, should a different lactam starting material be desired. For example, a cis-1-p-methoxyphenyl-3-acetoxy-4-phenylazetidin-2-one racemate prepared as above, in acetonitrile at a temperature such as -10° C. to -5° C., may be treated with a solution of ceric ammonium nitrate in water to yield a cis-3-acetoxy-4-phenylazetidin-2-one racemate. The latter compound may, for example, further be hydrolyzed, e.g., with aqueous potassium hydroxide, to yield cis-3-hydroxy-4-phenylazetidin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567614 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-ded21d337e2a41c299ec0d0226c06e7e |
| Source note | uspto-grants-1996_10 |