(E)-3-[4-(pyridin-3-ylmethyl)phenyl]allyl alcohol → 3-[4-(Pyridin-3-ylmethyl)phenyl]propanol

HRID 569145Notes

Reaction equation

HRID 569145 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]2[CH:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[CH2:16][OH:17])=[CH:10][CH:9]=2)[CH:2]=1.[H][H]>C(O)C.[C].[Pd]>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]2[CH:9]=[CH:10][C:11]([CH2:14][CH2:15][CH2:16][OH:17])=[CH:12][CH:13]=2)[CH:2]=1

Participants

5

Reactant 2

HCID 15594566(E)-3-[4-(pyridin-3-ylmethyl)phenyl]allyl alcoholHCID 178418361HCID 178418361, compound

Product 1

HCID 138227803-[4-(Pyridin-3-ylmethyl)phenyl]propanolYield 99.1%

Reagents, catalysts & solvents 2

HCID 178418390HCID 178418390, compoundCatalystHCID 702EthanolSolvent

Procedure

In 10 ml of ethanol was dissolved 500 mg of (E)-3-[4-(pyridin-3-ylmethyl)phenyl]allyl alcohol, and to the resulting solution was added 100 mg of 5% palladium-carbon, and the resulting mixture was stirred at room temperature in a hydrogen atmosphere for 2.5 hours. The reaction mixture thus obtained was filtered and the filtrate thus obtained was concentrated under reduced pressure to obtain 500 mg (yield 99.1%) of colorless, oily 3-[4-(pyridin-3-ylmethyl)phenyl]propanol.

Workup

  1. customThe reaction mixture thus obtained
  2. filtrationwas filtered
  3. customthe filtrate thus obtained
  4. concentrationwas concentrated under reduced pressure

Sources & evidence

ORD record
ord-8d428bae1cf941c2bd3464f16b9f2628
Source dataset
uspto-grants-1988_03
Patent number
US04731370

Reaction notes

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