HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyl-4-chlorobenzyl alcohol → 2-Benzyl-4-chlorobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyl-4-chlorobenzyl alcohol | HCID 15570066 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Benzyl-4-chlorobenzaldehyde | HCID 15570067 | — |
Reaction Steps
To a suspension of 238 g (1.1 mole) of pyridinium chlorochromate and 800 ml of methylene chloride was added 79.3 g (0.34-mole) of 2-benzyl-4-chlorobenzyl alcohol. The mixture was stirred at room temperature for 2 hr. The chromium salts were precipitated by the addition of 2.4 liters of 1:1 ether:petroleum ether, and the precipitate was removed by filtration through Celite. The solvent was removed at reduced pressure to give a yellow oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04379765 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-fb15ddd54eb24b52ace9dc9e5ae3bb5b |
| Source note | uspto-grants-1983_04 |