Friedel craft alkylation of toluene with vinyl chloride
Answers
Answered by
0
1-Arylalkenyl sulfides were produced in good yields by treatment of 1-(phenylthio)vinyl chlorides with arenes in the presence of aluminum chloride or ethylaluminum dichloride. The stereoselectivity indicated that the reaction is kinetically controlled process.
The Friedel-Crafts reaction of 1-(phenylthio)vinyl chlorides (1) with arenes proceeded in the presence of AlCl3 or EtAlCl2 to give 1-arylalkenyl sulfides (2). The stereoselectivity indicated that the reaction is a kinetically controlled process.
Web source
Answered by
1
Hey Dear,
◆ Friedel craft alkylation -
- It's aromatic nucleophilic substitution reaction.
- Presence of methyl group in ring favours Friedel craft reaction in toulene.
- Toluene on Friedel craft reaction with vinyl chloride gives 4-methyl-styrene.
Ph-CH3 + CH2=CH-Cl --> CH3-Ph-CH=CH2 + HCl
Hope this helped you. Thanks for asking questions.
Similar questions