Potassium Hydroxide → HCID 66666415, compound

HRID 1617950Notes

Reaction equation

HRID 1617950 reaction equation
[C:1]([C:4]1[CH:5]=[CH:6][C:7]([O:10][CH3:11])=[N:8][CH:9]=1)(=[O:3])[CH3:2].[Cl:12][C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([Cl:21])[CH:20]=1)[CH:16]=O.[OH-].[K+]>>[Cl:12][C:13]1[CH:14]=[C:15](/[CH:16]=[CH:2]/[C:1]([C:4]2[CH:9]=[N:8][C:7]([O:10][CH3:11])=[CH:6][CH:5]=2)=[O:3])[CH:18]=[C:19]([Cl:21])[CH:20]=1

Participants

4

Reactant 3

HCID 14797Potassium HydroxideHCID 357463,5-DichlorobenzaldehydeHCID 105348375-Acetyl-2-methoxypyridine

Product 1

HCID 66666415HCID 66666415, compound

Procedure

In analogy to example 170, step 1, 5-acetyl-2-methoxypyridine was reacted with 3,5-dichlorobenzaldehyde in the presence of potassium hydroxide to give the title compound as a colourless solid.

Sources & evidence

ORD record
ord-5f9839285d0b4d0493c64fba84196711
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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