HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl pivalate → Pivaloyloxymethyl 3-acetoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl pivalate | HCID 15916453 | — |
| Reactant | Sodium 3-acetoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate | HCID 23682168 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Pivaloyloxymethyl 3-acetoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate | HCID 20511949 | — |
Reaction Steps
A mixture of sodium 3-acetoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate (23 mg) and bromomethyl pivalate (29 mg) in hexamethylphosphoramide (0.5 ml) is stirred at room temperature and under a N2 atmosphere for 2.5 hrs. The mixture is diluted with toluene (10 ml), washed with H2O (5×2 ml) and brine, dried with MgSO4, filtered, and evaporated in vacuo. The residue is purified by silica gel plc to afford pivaloyloxymethyl 3-acetoxy-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369187 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-0cefbe7978ae464c84d1b6b1ee4e4765 |
| Source note | uspto-grants-1983_01 |