Friedel– Crafts alkylation

GPTKB entity

Statements (51)
Predicate Object
gptkbp:instance_of gptkb:chemical_compound
gptkbp:can_be_used_to_modify aromatic compounds
gptkbp:can_create multiple products
branched alkyl groups
linear alkyl groups
gptkbp:can_lead_to polyalkylation
aromatic hydrocarbons
gptkbp:design hydrolysis
gptkbp:has_limitations carbocation stability
https://www.w3.org/2000/01/rdf-schema#label Friedel– Crafts alkylation
gptkbp:involves alkyl halide
gptkbp:is_a_reaction_that_can_be_affected_by pressure
temperature
concentration of reactants
gptkbp:is_a_reaction_that_can_be_monitored_by NMR spectroscopy
GC-MS
gptkbp:is_a_reaction_that_can_be_optimized_for selectivity
yield
gptkbp:is_a_reaction_that_can_be_performed_in solvent-free conditions
gptkbp:is_a_reaction_that_can_be_performed_under anhydrous conditions
gptkbp:is_a_reaction_that_can_be_performed_with various alkyl groups
gptkbp:is_a_reaction_that_can_be_scaled_up_for industrial applications
gptkbp:is_a_reaction_that_can_produce complex mixtures
gptkbp:is_a_reaction_that_involves nucleophiles
electrophiles
gptkbp:is_affected_by reaction conditions
gptkbp:is_often_accompanied_by deprotection steps
gptkbp:is_often_used_in gptkb:pharmaceuticals
polymer chemistry
gptkbp:is_often_used_to_synthesize alkyl-substituted aromatics
gptkbp:is_used_in organic synthesis
gptkbp:key_feature aromatic chemistry
gptkbp:named_after gptkb:Charles_Friedel
James Crafts
gptkbp:performed_by benzene
naphthalene
toluene
gptkbp:produces alkylated aromatic compound
gptkbp:requires Lewis acid catalyst
gptkbp:sensitivity steric effects
gptkbp:suitable_for deactivated aromatic rings
gptkbp:type electrophilic aromatic substitution
gptkbp:type_of substitution reaction
gptkbp:was_a_catalyst_for BF3
Al Cl3
gptkbp:was_a_response_to synthesis of fragrances
synthesis of agrochemicals
synthesis of dyes
synthesis of polymers
gptkbp:bfsParent gptkb:Friedel–_Crafts_acylation
gptkbp:bfsLayer 8