Aniline → Tert-Butylbenzene
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1O)([CH3:4])([CH3:3])[CH3:2].NC1C=CC=CC=1>>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
Reactant 2
Product 1
Procedure
15 g (0.1 mol) of t-butylphenol, 6.31 g (0.21 mol) of p-formaldehyde and 10.24 g (0.11 mol) of aniline were added to a 100 ml one-neck round-bottom flask and mixed in an oil bath at 90° C. When the initially opaque mixture became a dark brown transparent gel type material after about 30 minutes, the reaction was quenched using tetrahydrofuran (THF), and then the mixture was cooled to room temperature. The cooled crude product was base-washed twice through a solvent extraction using a 1N NaOH aqueous solution, and washed once with deionized water. After washing, the organic layer was dried with MgSO4 and filtered. The residual solution was dried using a rotary evaporator to remove the solvent, and the purified product was dried in a vacuum oven at 40° C. for 6 hours to obtain t-BuPh-a.
Workup
- additionmixed in an oil bath at 90° C
- customafter about 30 minutes
- customthe reaction was quenched
- temperatureThe cooled crude product
- washwas base-washed twice through a solvent extraction
- washwashed once with deionized water
- washAfter washing
- dry with materialthe organic layer was dried with MgSO4
- filtrationfiltered
- customThe residual solution was dried
- customa rotary evaporator
- customto remove the solvent
- customthe purified product was dried in a vacuum oven at 40° C. for 6 hours
Sources & evidence
- ORD record
- ord-9624ea7e963d448e9d21772267560ddb
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08192892B2
Reaction notes
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