4-tert-Butylphenol → 2-(4-Chloro-alpha-cumyl)-4-tert-butylphenol

HRID 1281058Notes

Reaction equation

HRID 1281058 reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([CH3:8])=[CH2:7])=[CH:4][CH:3]=1.[C:11]([C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=1)([CH3:14])([CH3:13])[CH3:12]>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([C:19]2[CH:20]=[C:15]([C:11]([CH3:13])([CH3:12])[CH3:14])[CH:16]=[CH:17][C:18]=2[OH:21])([CH3:8])[CH3:7])=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 73934-tert-ButylphenolHCID 743814-Chloro-alpha-methylstyrene

Product 1

HCID 226643582-(4-Chloro-alpha-cumyl)-4-tert-butylphenol

Procedure

4-Chloro-α-methylstyrene (50 g) and 45 g of 4-tert-butylphenol are reacted according to the procedure of Example 3 to afford the title compound in a yield of 66.6 g as a colorless oil. The structure is confirmed by 1 Hnmr and mass spectroscopy.

Sources & evidence

ORD record
ord-6c66ca05b3e24fe2846222667485aa3b
Source dataset
uspto-grants-2002_09
Patent number
US06451887B1

Reaction notes

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