Acetic Anhydride → HCID 18707199, compound

HRID 1421978Notes

Reaction equation

HRID 1421978 reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[S:14][CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([OH:24])=[C:20]([C:25]([OH:27])=[O:26])[CH:19]=3)[N:17]=2)[CH:7]=[CH:8][C:9]=1[O:10][CH2:11][CH3:12])[CH3:2].[C:28](OC(=O)C)(=[O:30])[CH3:29]>>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[S:14][CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([O:24][C:28](=[O:30])[CH3:29])=[C:20]([C:25]([OH:27])=[O:26])[CH:19]=3)[N:17]=2)[CH:7]=[CH:8][C:9]=1[O:10][CH2:11][CH3:12])[CH3:2]

Participants

3

Procedure

A solution of 1 g of 2-(3,4-diethoxyphenyl)-4-(3-carboxy-4-hydroxyphenyl)thiazole in 5 ml of acetic anhydride was stirred at 100° C. for 4 hours with heating. The solvent was distilled off. The residue was dissolved in 50 ml of ethyl acetate. To the solution was added 10 ml of a saturated sodium hydrogencarbonate solution, and phase separation was conducted. The ethyl acetate layer was made acidic with 10% hydrochloric acid, washed with 10 ml of a saturated aqueous sodium chloride solution, dried and subjected to distillation to remove the solvent. The residue was recrystallized from ethyl acetate to obtain 145 mg of 2-(3,4-diethoxyphenyl)-4-(3-carboxy-4-acetyloxyphenyl)thiazole.

Workup

  1. temperaturewith heating
  2. distillationThe solvent was distilled off
  3. dissolutionThe residue was dissolved in 50 ml of ethyl acetate
  4. additionTo the solution was added
  5. custom10 ml of a saturated sodium hydrogencarbonate solution, and phase separation
  6. washwashed with 10 ml of a saturated aqueous sodium chloride solution
  7. customdried
  8. distillationsubjected to distillation
  9. customto remove the solvent
  10. customThe residue was recrystallized from ethyl acetate

Sources & evidence

ORD record
ord-dd7e821a0aed4218bad43cdc621ae9f0
Source dataset
uspto-grants-2000_06
Patent number
US06080764

Reaction notes

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