HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | (p-Chlorophenyl)trmethylsilane | HCID 66351 | — |
| Product | Benzophenone | HCID 3102 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042613 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-db5dedecb7c54d88aad0b11177dd94ea |
| Source note | uspto-grants-1977_08 |