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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982151Generated: November 1, 2026

Acetyl chloride → HCID 20069224, compound

https://huagongshe.com/reaction/982151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant1,1-DiphenylethaneHCID 11918—
ReactantHCID 21696373HCID 21696373—
ProductHCID 20069224HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994539
Source datasetuspto-grants-1991_02
ORD IDord-c89ac98360e843c99d77f82aa1d105c1
Source noteuspto-grants-1991_02