HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Benzoylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | α1-Phenyl-1,2-benzenedimethanol | HCID 11424431 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Benzoylbenzaldehyde | HCID 161195 | — |
Reaction Steps
A mixture of 1 g. of selenium dioxide and 1 g. of 2-hydroxymethylbenzhydrol in 5 ml. of acetic acid was refluxed for 41/2 hours. The solution was cooled, filtered from selenium and the filtrate was poured into ice water and made alkaline with sodium hydroxide. Extraction with ether gave a yellow oil to which petroleum ether was added. White prisms were obtained which melted at 64°-67°. Ultraviolet maximum (2-propanol) at 226/7 mμ (ε = 15,750) and 251/2 mμ (ε = 18,500), inflexion at 294 mμ (ε = 2600); infrared absorption (CHCl3) at 1665 cm-1 and 1705 cm-1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931217 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-dbd46268722e4ab7aa321afdae17c09e |
| Source note | uspto-grants-1976_01 |