Gallic Acid → phenyl gallate
Reaction equation
[C:1]([OH:12])(=[O:11])[C:2]1[CH:10]=[C:8]([OH:9])[C:6]([OH:7])=[C:4]([OH:5])[CH:3]=1.[C:13]1(O)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.P(Cl)(Cl)(Cl)=O>CCOCC>[C:1]([O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)(=[O:11])[C:2]1[CH:10]=[C:8]([OH:9])[C:6]([OH:7])=[C:4]([OH:5])[CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A reaction mixture was prepared containing 15 g. of anhydrous gallic acid, 8 g. of phenol, 4 ml. of phosphorous oxychloride and 200 ml. of anhydrous ether in a round-bottom flask. The mixture was heated to refluxing temperature for about 18 hours. The ether solvent was removed by evaporation. Water was added to the resulting residue and the pH of the aqueous layer adjusted to about 5 by the addition of dilute aqueous sodium hydroxide. Phenyl gallate, being insoluble at pH=5, separated and was extracted with ether. The ether extracts were separated and dried and the ether removed therefrom by evaporation. Recrystallization of the residue yielded phenyl gallate melting at about 190°-191° C.
Workup
- customA reaction mixture was prepared
- additioncontaining 15 g
- temperatureThe mixture was heated
- temperatureto refluxing temperature for about 18 hours
- customThe ether solvent was removed by evaporation
- additionWater was added to the resulting residue
- additionthe pH of the aqueous layer adjusted to about 5 by the addition of dilute aqueous sodium hydroxide
- customseparated
- extractionwas extracted with ether
- customThe ether extracts were separated
- customdried
- customthe ether removed
- customby evaporation
- customRecrystallization of the residue
Sources & evidence
- ORD record
- ord-b1edb21e09d84229bed7700348bdee09
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04448730
Reaction notes
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