Catechol → o-[p-(4-Phenylbutoxy)benzyloxy]phenol

HRID 1197091Notes

Reaction equation

HRID 1197091 reaction equation
Cl[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:5][CH:4]=1.[C:20]1([C:22](=[CH:24][CH:25]=[CH:26][CH:27]=1)[OH:23])[OH:21].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.O>[C:14]1([CH2:13][CH2:12][CH2:11][CH2:10][O:9][C:6]2[CH:7]=[CH:8][C:3]([CH2:2][O:21][C:20]3[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=3[OH:23])=[CH:4][CH:5]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

6

Reactant 3

HCID 289CatecholHCID 11430Potassium CarbonateHCID 151155321-(Chloromethyl)-4-(4-phenylbutoxy)benzene

Product 1

HCID 19882704o-[p-(4-Phenylbutoxy)benzyloxy]phenolYield 48.5%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

In 1.5 ml of N,N-dimethylformamide were stirred 390 mg of 4-chloromethyl-1-(4-phenylbutoxy)benzene, 180 mg of catechol and 270 mg of potassium carbonate at room temperature overnight. The reaction mixture was dispersed in water and ethyl acetate and the dispersion was separated. The ethyl acetate layer washed subsequently with water and an aqueous saline solution, dried and concentrated. The obtained residue was applied to silica gel column chromatography and eluted with toluene to obtain 240 mg of o-[p-(4-phenylbutoxy)benzyloxy]phenol.

Workup

  1. customethyl acetate and the dispersion was separated
  2. washThe ethyl acetate layer washed subsequently with water
  3. customan aqueous saline solution, dried
  4. concentrationconcentrated
  5. washeluted with toluene

Sources & evidence

ORD record
ord-3029ad5d7c5148e88ad70c6876927f48
Source dataset
uspto-grants-1992_05
Patent number
US05116853

Reaction notes

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