Phenol → HCID 13326123, compound

HRID 746306Notes

Reaction equation

HRID 746306 reaction equation
[Cl:1][C:2]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:3]=1[O:4][C:5]#[C:6][C:7]([CH3:10])([CH3:9])[CH3:8].[Cl:16][C:17]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=1[OH:24].C1(O)C=CC=CC=1>[Cl-].[Zn+2].[Cl-]>[Cl:1][C:2]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:3]=1[O:4][C:5]([O:24][C:18]1[CH:19]=[CH:20][C:21]([Cl:23])=[CH:22][C:17]=1[Cl:16])=[CH:6][C:7]([CH3:10])([CH3:9])[CH3:8]

Participants

5

Reactant 3

HCID 996PhenolHCID 84492,4-DichlorophenolHCID 135748772,4-Dichloro-1-[(3,3-dimethylbut-1-yn-1-yl)oxy]benzene

Product 1

HCID 13326123HCID 13326123, compound

Reagents, catalysts & solvents 1

HCID 3007855ZincchlorideCatalyst

Conditions

Temperature
160 °C

Procedure

24.3 g (0.1 mole) of 1-(2,4-dichlorophenoxy)-3,3-dimethylbut-1-yne were initially taken together with 16.3 g (0.1 mole) of 2,4-dichlorophenol and 1.4 g (0.01 mole) of zinc chloride, and the stirred mixture was heated at 160° C. After 30 minutes, the phenol had reacted quantitatively with the phenoxyalkyne to give 1,1-bis-(2,4-dichlorophenoxy)-3,3-dimethylbut-1-ene.

Sources & evidence

ORD record
ord-befaf93dc49e4b73a850249b489e376d
Source dataset
uspto-grants-1986_07
Patent number
US04603224

Reaction notes

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