Acetyl chloride → HCID 20069224, compound

HRID 982151Notes

Reaction equation

HRID 982151 reaction equation
[C:1]1([CH:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[CH:15]=[CH2:16])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(C(C2C=CC=CC=2)C)C=CC=CC=1.C(Cl)(=[O:33])C>>[C:1]1([CH:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15](=[O:33])[CH3:16])[CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

4

Reactant 3

HCID 6367Acetyl chlorideHCID 119181,1-DiphenylethaneHCID 21696373HCID 21696373, compound

Product 1

HCID 20069224HCID 20069224, compound

Procedure

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.

Workup

  1. customThey can be prepared by a variety of chemical synthetic manners

Sources & evidence

ORD record
ord-c89ac98360e843c99d77f82aa1d105c1
Source dataset
uspto-grants-1991_02
Patent number
US04994539

Reaction notes

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