Potassium Carbonate → Benzyl 3-(2-azidoethyloxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate
Reaction equation
[N:1]12[C:7](=[O:8])[CH2:6][CH:5]1[CH2:4][C:3](=[O:9])[CH:2]2[C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11].FC(S(O[CH2:28][CH2:29][N:30]=[N+:31]=[N-:32])(=O)=O)(F)F.C(=O)([O-])[O-].[K+].[K+]>C=C.CCOCC>[N:30]([CH2:29][CH2:28][O:9][C:3]1[CH2:4][CH:5]2[N:1]([C:7](=[O:8])[CH2:6]2)[C:2]=1[C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11])=[N+:31]=[N-:32]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 25 °C
Procedure
A mixture of benzyl 1-azabicyclo[3.2.0]heptane-3,7-dione-2-carboxylate (26 mg) and 2-azidoethyl trifluoromethyl sulfonate (26 mg) in anhydrous acetene (0.5 ml) containing powdered potassium carbonate (28 mg) is stirred at 25° C. in a capped flask for 2 hrs. The mixture is diluted with anhydrous ether (5 ml) and filtered. The filtrate is washed with water (2 ml) and brine, dried with MgSO4, filtered, and evaporated in vacuo. The residue is purified by plc on a silica gel GF plate to afford benzyl 3-(2-azidoethyloxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate.
Workup
- filtrationfiltered
- washThe filtrate is washed with water (2 ml) and brine
- dry with materialdried with MgSO4
- filtrationfiltered
- customevaporated in vacuo
- customThe residue is purified by plc on a silica gel GF plate
Sources & evidence
- ORD record
- ord-ff84bcf4c4c04fd0ab0b30c53b437e1d
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04318912
Reaction notes
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