Acetophenone → HCID 491437, compound

HRID 1402900Notes

Reaction equation

HRID 1402900 reaction equation
[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1[CH:4]=O.[C:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)(=[O:13])[CH3:12]>>[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[CH:12][C:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:13]

Participants

3

Reactant 2

HCID 7410AcetophenoneHCID 134042,4-Dichlorobenzaldehyde

Product 1

HCID 491437HCID 491437, compound

Procedure

By a procedure similar to that of example 1.59.1, starting from 2,4-dichlorobenzaldehyde and acetophenone, 3-(2,4-dichlorophenyl)-1-phenylprop-2-en-1-one was obtained as yellow solid.

Sources & evidence

ORD record
ord-fa2a3e96d4254d71932b1dceb2f072ea
Source dataset
uspto-grants-2014_12
Patent number
US08912186B2

Reaction notes

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