Hydrochloric Acid → HCID 70299391, compound

HRID 1378413Notes

Reaction equation

HRID 1378413 reaction equation
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH2:12][CH2:13][CH:14]=[C:15]2[C:28]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[S:22][C:21]3[C:16]2=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:7]1)=[O:5])C.[OH-].[Na+].Cl.[Cl:32]CCl>C(O)C>[ClH:32].[CH:17]1[C:16]2[C:15](=[CH:14][CH2:13][CH2:12][N:8]3[CH2:9][CH2:10][CH2:11][CH:6]([C:4]([OH:5])=[O:3])[CH2:7]3)[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[S:22][C:21]=2[CH:20]=[CH:19][CH:18]=1

Participants

6

Procedure

The above ester (0.74 g, 1.8 mmol) was dissolved in ethanol (25 ml) and 40% sodium hydroxide (6 ml) was added. The mixture was heated at reflux for 1 h. 10% Hydrochloric acid (25 ml) was added followed by dichloromethane (150 ml). The phases were separated and the organic phase was washed with water, dried (NaSO4) and the solvent was evaporated in vacuo to give 0.6 g of the title compound as a solid. M.p. 150°-160° C. A sample was dissolved in acetone and precipitated with diethyl ether. The solid formed was isolated by filtration and dried in vacuo.

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 1 h
  3. customThe phases were separated
  4. washthe organic phase was washed with water
  5. dry with materialdried (NaSO4)
  6. customthe solvent was evaporated in vacuo

Sources & evidence

ORD record
ord-736f1922694d43ca84cc98118fc6521c
Source dataset
uspto-grants-1997_09
Patent number
US05668129

Reaction notes

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