Lithium Hydroxide → HCID 178497118, compound

HRID 1634307Notes

Reaction equation

HRID 1634307 reaction equation
C[O:2][C:3](=[O:29])[C:4]([OH:28])=[CH:5][C:6]([C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH2:18][O:19][CH3:20])[CH:15]=2)[N:10]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH:9]=1)=[O:7].[OH-].[Li+]>O1CCOCC1>[C:24]([O:23][C:21]([N:10]1[C:11]2[C:16](=[CH:15][C:14]([O:17][CH2:18][O:19][CH3:20])=[CH:13][CH:12]=2)[C:8]([C:6](=[O:7])[CH:5]=[C:4]([OH:28])[C:3]([OH:29])=[O:2])=[CH:9]1)=[O:22])([CH3:27])([CH3:25])[CH3:26]

Participants

4

Procedure

To a solution of 0.345 g (0.85 mmol) of the ester derivative obtained in above (1) in dioxane (7 ml) was added 1.7 ml of 1 N lithium hydroxide. The mixture was stirred for 1.5 hours at room temperature. The solvent was removed under reduced pressure at room temperature and the residue was dissolved in water. The aqueous layer was washed twice with ethyl acetate and neutralized with 1 N hydrochloric acid (1.7 ml) and extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried. The solvent was removed and the obtained crystal was washed with ethyl acetate to give 0.28 g of the titled compound. Yield: 84%. m.p.: 165-170° C. (decomposition)

Workup

  1. customThe solvent was removed under reduced pressure at room temperature
  2. dissolutionthe residue was dissolved in water
  3. washThe aqueous layer was washed twice with ethyl acetate and neutralized with 1 N hydrochloric acid (1.7 ml)
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with water and brine
  6. customdried
  7. customThe solvent was removed
  8. washthe obtained crystal was washed with ethyl acetate

Sources & evidence

ORD record
ord-6df93c2be24f440187c37899a692b036
Source dataset
uspto-grants-2003_01
Patent number
US06506787B2

Reaction notes

Loading…