Hydrochloric Acid → (1-Chloro-1-methylethyl)benzene

HRID 1252743Notes

Reaction equation

HRID 1252743 reaction equation
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[CH2:3].[ClH:10]>C(Cl)Cl>[C:2]([Cl:10])([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)([CH3:1])[CH3:3]

Participants

4

Procedure

183 g of α-methyl styrene, dissolved in 600 ml of methylene chloride, were reacted with hydrogen chloride at a temperature of from -12 to -10° C. to yield α-cumyl chloride. The resulting solution was added dropwise at a temperature of -10° C. to a mixture of 3 g of anhydrous aluminum trichloride, 12 g of anhydrous iron trichloride, 0.5 g of phosphorus pentoxide and 1800 ml of methylene chloride in the course of 60 minutes, and the mixture was then stirred at -10° C. for a further 4 hours. To terminate the reaction, the reaction mixture was poured into 6 liters of water at room temperature.

Sources & evidence

ORD record
ord-aa96d0f0438144c995c04de5c8baa6b3
Source dataset
uspto-grants-1988_05
Patent number
US04745176

Reaction notes

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