Toluene → p-METHYLACETOPHENONE
Reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[C:5]1([CH3:11])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>C(=S)=S>[C:5]1([CH3:11])[CH:10]=[CH:9][C:8]([C:12](=[O:14])[CH3:13])=[CH:7][CH:6]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Anhydrous aluminum chloride (89.6 g, 0.67 mol) was added to a solution of toluene (28.5 g, 0.31 mol) in 120 mL of dry carbon disulfide. The mixture was heated to reflux and acetic anhydride (24.5 g, 0.24 mol) was added over one hour. Heating was continued for an additional hour. The solvent was removed by distillation. The reaction mixture was cooled and slowly poured into a well-stirred mixture of ice and hydrochloric acid. The mixture was extracted several times with ether. The combined extracts were washed with water and 10% sodium hydroxide, dried over calcium chloride, filtered, and the solvent was removed. Distillation gave the desired product 1-p-tolyl-ethanone (27.08 g). 1E1 NMR (300 MHz, DMSO-d6) δ 2.36 (s, 3H), 2.50 (s, 3H), 7.32 (d, 2H), 7.85 (d, 2H); ELMS (M+): 134.
Workup
- temperatureThe mixture was heated
- temperatureto reflux
- temperatureHeating
- waitwas continued for an additional hour
- customThe solvent was removed by distillation
- temperatureThe reaction mixture was cooled
- additionslowly poured into a well-stirred mixture of ice and hydrochloric acid
- extractionThe mixture was extracted several times with ether
- washThe combined extracts were washed with water and 10% sodium hydroxide
- dry with materialdried over calcium chloride
- filtrationfiltered
- customthe solvent was removed
- distillationDistillation
Sources & evidence
- ORD record
- ord-2aeb157c57bf4318a9c7c09ffc5b1009
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08101633B2
Reaction notes
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