HCID 14329809, compound → 2-((E)-4-methoxybenzylidene)butan-1-al

HRID 2231304Notes

Reaction equation

HRID 2231304 reaction equation
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6](/[CH:7]=[C:8](\[CH2:11][CH3:12])/[CH2:9][OH:10])=[CH:5][CH:4]=1>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6](/[CH:7]=[C:8](\[CH2:11][CH3:12])/[CH:9]=[O:10])=[CH:5][CH:4]=1

Participants

4

Reactant 1

HCID 14329809HCID 14329809, compound

Product 1

HCID 136347482-((E)-4-methoxybenzylidene)butan-1-alYield 73.1%

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 6212ChloroformSolvent

Procedure

A mixture of 2-((E)-4-methoxybenzylidene)butan-1-ol (13 g) and manganese dioxide (130 g) in chloroform (600 ml) was stirred at room temperature for 20 hours. Manganese dioxide was filtered off by filtration and the filtrate was condensed to give 2-((E)-4-methoxybenzylidene)butan-1-al (9.4 g).

Workup

  1. filtrationManganese dioxide was filtered off by filtration
  2. customcondensed

Sources & evidence

ORD record
ord-a7ba023c632048f795faa9af0023771f
Source dataset
uspto-grants-1988_11
Patent number
US04782088

Reaction notes

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