Potassium Carbonate → HCID 86751149, compound

HRID 2257244Notes

Reaction equation

HRID 2257244 reaction equation
[C:1]([CH2:8][CH2:9][CH:10]([NH2:31])[C:11]([O:22][C:23](=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)([C:17]([O:19][CH2:20]C)=[O:18])[C:12]([O:14][CH2:15]C)=[O:13])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C([O-])([O-])=O.[K+].[K+]>CO>[C:23]([O:22][CH3:11])(=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[C:1]([CH2:8][CH2:9][CH:10]([NH2:31])[C:11]([OH:22])([C:12]([O:14][CH3:15])=[O:13])[C:17]([O:19][CH3:20])=[O:18])([O:3][C:4]([CH3:6])([CH3:5])[CH3:7])=[O:2]

Participants

5

Procedure

A mixture of 4 g of ethyl 5-BOC-amino-2-benzoyloxy-2-ethoxycarbonyl-pentanoate and 2 g of K2CO3 in 40 ml of anhydrous methanol, cooled to 0°-5° C., is stirred for 1 h. After filtration of the potassium carbonate excess, the solution is acidified to pH 6 with 2N HCl and filtered from the salts which separate. Solvent is evaporated off under vacuum and the residue is partitioned between cold water and ethyl acetate. The organic phase is washed repeatedly with a 5% K2CO3 cold solution and with water to neutrality, dried over sodium sulfate and evaporated to dryness. The residue (3 g) is eluted, purified on 30 g of silica gel, eluent hexane-ethyl acetate from 95:5 to 80:20, to give methyl benzoate and 1.8 g of methyl 5-BOC-amino-2-hydroxy-2-methoxycarbonyl-pentanoate (oil).

Workup

  1. temperaturecooled to 0°-5° C.
  2. filtrationAfter filtration of the potassium carbonate excess
  3. filtrationfiltered from the salts which
  4. customseparate
  5. customSolvent is evaporated off under vacuum
  6. customthe residue is partitioned between cold water and ethyl acetate
  7. washThe organic phase is washed repeatedly with a 5% K2CO3 cold solution and with water to neutrality
  8. dry with materialdried over sodium sulfate
  9. customevaporated to dryness
  10. washThe residue (3 g) is eluted
  11. custompurified on 30 g of silica gel, eluent hexane-ethyl acetate from 95:5 to 80:20

Sources & evidence

ORD record
ord-ada869a4273144778fc513c70f9fc59c
Source dataset
uspto-grants-1997_08
Patent number
US05656656

Reaction notes

Loading…