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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164694Generated: November 1, 2026

1-Naphthaldehyde → HCID 20069224, compound

https://huagongshe.com/reaction/2164694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantAcetyl chlorideHCID 6367—
Reactant1,1-DiphenylethaneHCID 11918—
Reactant1-VinylnaphthaleneHCID 70004—
ReactantHCID 178418373HCID 178418373—
ProductHCID 20069224HCID 20069224—
ProductHCID 21696373HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04506107
Source datasetuspto-grants-1985_03
ORD IDord-b4ca470edea3478bbb7a77afc5ddb51f
Source noteuspto-grants-1985_03