HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 20069224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,1-Diphenylethane | HCID 11918 | — |
| Reactant | HCID 21696373 | HCID 21696373 | — |
| Product | HCID 20069224 | HCID 20069224 | — |
Reaction Steps
These compounds can be prepared through various chemical synthesis methods. For example, phenyl(vinylphenyl)ethane is prepared by reacting diphenylethane with acetyl chloride in the presence of Friedel-Crafts catalyst to obtain phenyl(acetylphenyl)ethane, then it is reduced with sodium borohydride and dehydrated. Phenyl(isopropenylphenyl)ethane is prepared by reacting phenyl(formylpheny)ethane with a Grignard reagent such as methylmagnesium iodide, which is followed by dehydration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04543207 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-44f53c32f85b4abb81ed640cd9a806ab |
| Source note | uspto-grants-1985_09 |