Potassium Carbonate → Benzyl 3-(2-azidoethyloxy)-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylate

HRID 1164343Notes

Reaction equation

HRID 1164343 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

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

  1. filtrationfiltered
  2. washThe filtrate is washed with water (2 ml) and brine
  3. dry with materialdried with MgSO4
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customThe residue is purified by plc on a silica gel GF plate

Sources & evidence

ORD record
ord-c544158922cb487b96421ea70454a174
Source dataset
uspto-grants-1983_01
Patent number
US04369187

Reaction notes

Loading…