Allyl chloride → 4-[4-(4-Pyridyl)piperazin-1-yl]phenol allyl ether

HRID 266766Notes

Reaction equation

HRID 266766 reaction equation
[H-].[Na+].[N:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=3)[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.[CH2:22](Cl)[CH:23]=[CH2:24]>CN(C=O)C>[CH2:24]([O:21][C:18]1[CH:19]=[CH:20][C:15]([N:12]2[CH2:11][CH2:10][N:9]([C:6]3[CH:7]=[CH:8][N:3]=[CH:4][CH:5]=3)[CH2:14][CH2:13]2)=[CH:16][CH:17]=1)[CH:23]=[CH2:22]

Participants

5

Reactant 3

HCID 7850Allyl chlorideHCID 24758Sodium hydrideHCID 149869034-(4-(4-Pyridyl)piperazin-1-yl)phenol

Product 1

HCID 571157974-[4-(4-Pyridyl)piperazin-1-yl]phenol allyl etherYield 85.7%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Sodium hydride (60% dispersion in mineral oil, 0.4 g) was added to a stirred suspension of 4-[4-(4-pyridyl)piperazin-1-yl]phenol (2.55 g) in DMF (25 ml) and the mixture stirred for 20 minutes at room temperature. Allyl chloride (0.756 g) was added dropwise and stirring continued for 20 hours. Ice-water (75 ml) was added and the mixture extracted three times with ethyl acetate. The combined extracts were washed with water and brine, dried (MgSO4) and evaporated. The residue was triturated with hexane and filtered to give 4-[4-(4-pyridyl)piperazin-1-yl]phenol allyl ether (2.5 g) as a solid; NMR(d6DMSO) δ 8.18(2H,dd), 6.8-7.0(6H,m), 5.92-6.13(1H,m), 5.2-5.45(2H,m), 4.5(2H,m), 3.45(4H,m), 3.11(4H,m).

Workup

  1. stirringstirring
  2. waitcontinued for 20 hours
  3. extractionthe mixture extracted three times with ethyl acetate
  4. washThe combined extracts were washed with water and brine
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue was triturated with hexane
  8. filtrationfiltered

Sources & evidence

ORD record
ord-85d9ef5ea3d8400c81eb8eb17ac85b53
Source dataset
uspto-grants-1997_07
Patent number
US05652242

Reaction notes

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