HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 3-(alpha-azidoacetoxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-azidoacetyl Chloride | HCID 10909558 | — |
| Reactant | Benzyl 3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate | HCID 12804725 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-(alpha-azidoacetoxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate | HCID 15136298 | — |
Reaction Steps
Azidoacetyl chloride (21 μl) is added by syringe in an ice-cold, stirring solution of triethylamine (42 μl) and benzyl 1-azabicyclo[3.2.0]heptane-3,7-dione-2-carboxylate (52 mg) in anhydrous methylene chloride (2 ml). After stirring 30 mins in the cold, the reaction mixture is diluted with methylene chloride (5 ml), washed with H2O (2 ml), pH 3 phosphate buffer (2 ml), and 5% NaHCO3 (2 ml), dried with MgSO4, filtered, and evaporated in vacuo. Chromatography of the residue on a silica gel GF plate gives benzyl 3-(α-azidoacetoxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021566 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-9d9b84cbc4b44e7f83a235f06aa47389 |
| Source note | uspto-grants-1991_06 |