Acetyl chloride → HCID 20069224, compound

HRID 1719848Notes

Reaction equation

HRID 1719848 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

These compounds can be prepared through various chemical synthesis methods. For example, phenyl(vinylphenyl)ethane is prepared by reacting diphenylethane with acetyl chloride in the presence of Friedel-Crafts catalyst to obtain phenyl(acetylphenyl)ethane, then it is reduced with sodium borohydride and dehydrated. Phenyl(isopropenylphenyl)ethane is prepared by reacting phenyl(formylpheny)ethane with a Grignard reagent such as methylmagnesium iodide, which is followed by dehydration.

Workup

  1. customThese compounds can be prepared through various chemical synthesis methods

Sources & evidence

ORD record
ord-44f53c32f85b4abb81ed640cd9a806ab
Source dataset
uspto-grants-1985_09
Patent number
US04543207

Reaction notes

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