Acetic Anhydride → HCID 18707199, compound
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
- temperaturewith heating
- distillationThe solvent was distilled off
- dissolutionThe residue was dissolved in 50 ml of ethyl acetate
- additionTo the solution was added
- custom10 ml of a saturated sodium hydrogencarbonate solution, and phase separation
- washwashed with 10 ml of a saturated aqueous sodium chloride solution
- customdried
- distillationsubjected to distillation
- customto remove the solvent
- 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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