Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,1-Diphenylethane | HCID 11918 | — |
| Reactant | 1-Vinylnaphthalene | HCID 70004 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Product | HCID 20069224 | HCID 20069224 | — |
| Product | HCID 21696373 | HCID 21696373 | — |
Reaction Steps
For instance, vinylnaphthalene is prepared by reacting formylnaphthalene with a Grignard reagent such as methylmagnesium iodide, and then dehydrating. Phenyl(vinylphenyl)ethane is prepared by reacting diphenylethane with acetyl chloride in the presence of a Friedel-Crafts catalyst to obtain phenyl(acetylphenyl)ethane, reducing by sodium borohydride, and then dehydrating. Phenyl(isopropenylphenyl)ethane is prepared by reacting phenyl(acetylphenyl)ethane with a Grignard reagent such as methylmagnesium iodide, and then dehydrating. 1,2-Diphenylethylene is prepared by reacting benzaldehyde with benzylmagnesium bromide, and then dehydrating. 1,2-Diphenylpropene is also prepared by a similar method. 1,1-Diphenylethylene is prepared by reacting diphenyl ketone with a Grignard reagent such as methylmagnesium iodide, and then dehydrating.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04506107 |
|---|
| Source dataset | uspto-grants-1985_03 |
|---|
| ORD ID | ord-b4ca470edea3478bbb7a77afc5ddb51f |
|---|
| Source note | uspto-grants-1985_03 |
|---|