Phenyl phenylglyoxylate → Phenyl benzoate
Reaction equation
[C:1]1([C:7](=O)[C:8]([O:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3]C=1>[Cl-].C1([P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Cl)(Cl)Cl>[C:8]([O:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)(=[O:9])[C:7]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:1]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The decarbonylation reaction of phenyl phenylglyoxylate (PPG) was repeated in the manner as described in Example 79, except that neither tetraphenylphosphonium chloride nor chloroform was employed. The results are also set forth in Table 12.
Sources & evidence
- ORD record
- ord-9fbbfbfddd16461f95e28fccac4f61d6
- Source dataset
- uspto-grants-1999_04
- Patent number
- US05892091
Reaction notes
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