Benzaldehyde → Benzophenone
Reaction equation
[CH:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C)[C:11]1[CH:18]=[CH:17][C:14](C=O)=[CH:13][CH:12]=1.C[Si](C)(C)C1C=CC(Cl)=CC=1>>[C:1]([C:11]1[CH:18]=[CH:17][CH:14]=[CH:13][CH:12]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
Various benzophenone derivatives were prepared in accordance with the same procedure as in Example 1 excepting that 0.2 mole of a benzaldehyde derivative was used instead of 4-dimethylaminobenzaldehyde and 0.2 mole of a halobenzene derivative was used instead of 4-trimethylsilylchlorobenzene. The particulars are set out as follows.
Sources & evidence
- ORD record
- ord-db5dedecb7c54d88aad0b11177dd94ea
- Source dataset
- uspto-grants-1977_08
- Patent number
- US04042613
Reaction notes
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