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
They can be prepared by a variety of chemical synthetic manners, and for example, phenyl-(vinylpheny)ethane may be prepared by reacting diphenylethane with acetyl chloride in the presence of a Friedel-Crafts catalyst to form phenyl(acetylphenyl)ethane, reducing the latter with sodium boron hydrine or the like, and dehydrating it. Phenyl(isopropenylphenyl)ethane can be prepared by reacting phenyl(formylphenyl)ethane with a Grignard reagent such as methylmagnesium iodide, and carrying out dehydration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994539 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-c89ac98360e843c99d77f82aa1d105c1 |
| Source note | uspto-grants-1991_02 |