Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11118256 | HCID 11118256 | — |
| Reactant | HCID 57320287 | HCID 57320287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86742436 | HCID 86742436 | — |
Reaction Steps
A solution of 0.71 ml of triethylamine and 1.1 g of p-nitrobenzyloxyoxalyl chloride in 10 ml of methylene chloride was added to a solution of 0.9 g of (3S,4S)-3-[(1R)-1-trimethylsilyloxyethyl]-4-[(1RS)-1-(phenylthiocarbonyl)ethyl]-2-azetidinone in 10 ml of methylene chloride, cooled to about -30° C., and the mixture was stirred for 35 minutes at the same temperature. The reaction mixture was worked up and purified in the same manner as in Preparation 1(3), giving (3S,4S)-3-[(1R)-1-trimethylsilyloxyethyl]-4-[(1RS)-1-(phenylthiocarbonyl)ethyl]-1-(p-nitrobenzyloxyoxalyl)-2-azetidinone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04771046 |
|---|
| Source dataset | uspto-grants-1988_09 |
|---|
| ORD ID | ord-6cf758bcb87b423abe6af37b44104b07 |
|---|
| Source note | uspto-grants-1988_09 |
|---|