p-Toluenesulfonic acid → HCID 14988334, compound

HRID 846627Notes

Reaction equation

HRID 846627 reaction equation
[C:1]([O:4][CH2:5]/[CH:6]=[CH:7]\[C:8]1[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=1)(=[O:3])[CH3:2].C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH:26]([O:28][CH2:29][CH3:30])=[CH2:27]>CCOCC>[C:1]([O:4][CH2:5]/[CH:6]=[CH:7]\[C:8]1[CH:9]=[CH:10][C:11]([O:14][CH:26]([O:28][CH2:29][CH3:30])[CH3:27])=[CH:12][CH:13]=1)(=[O:3])[CH3:2]

Participants

5

Procedure

To 50 ml of methanol solution containing 10 g of 3-[4-(1-ethoxyethoxy)phenyl]propargyl acetate, were added 1.5 g of 5%-Pd-BaSO4 and 10 drops of quinoline, and the mixture was catalytically reduced. After the reaction was finished, the reaction mixture was filtered, and the filtrate was allowed to evaporation, the residue thus obtained was purified by means of a silica gel column chromatography (eluent: dichloromethane and dichloromethane:methanol=100:1) to obtain 3 g of 4(Z)-(1-ethoxyethoxy)cinnamyl acetate and 4 g of 4(Z)-hydroxycinnamyl acetate. Thus obtained 4 g of 4(Z)-hydroxycinnamyl acetate was dissolved in 20 ml of anhydrous ether, to this solution was added 50 mg of p-toluenesulfonic acid and 10 ml of ethyl vinyl ether, and the whole mixture was refluxed for 3 hours. The reaction mixture was then washed with 5%-sodium hydroxide aqueous solution and water in this order, and dried. The solvent was removed by evaporation to yield 4.8 g of 4(Z)-(1-ethoxyethoxy)cinnamyl acetate.

Workup

  1. temperaturethe whole mixture was refluxed for 3 hours
  2. washThe reaction mixture was then washed with 5%-sodium hydroxide aqueous solution and water in this order
  3. customdried
  4. customThe solvent was removed by evaporation

Sources & evidence

ORD record
ord-48703bf66d22452e981eab2426a649d7
Source dataset
uspto-grants-1992_08
Patent number
US05137889

Reaction notes

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