Hydrochloric Acid → HCID 68682751, compound
Reaction equation
[F:1][C:2]([F:19])([F:18])[O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[O:11])=[CH:6][CH:5]=1.[ClH:20]>C(O)C>[ClH:20].[F:18][C:2]([F:1])([F:19])[O:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[O:11])=[CH:8][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 20.0 grams (0.075 mole) of 4-pyridyl 4-(trifluoromethoxy)phenyl ketone in 350 mL of ethanol was stirred as hydrogen chloride gas was bubbled through during a five minute period. Upon completion of addition, the reaction mixture was stirred for one hour, and then it was filtered to collect a solid. The solid was washed with three portions of diethyl ether, and dried in a vacuum oven, yielding about 22.0 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Workup
- customwas bubbled through during a five minute period
- additionUpon completion of addition
- filtrationit was filtered
- customto collect a solid
- washThe solid was washed with three portions of diethyl ether
- customdried in a vacuum oven
Sources & evidence
- ORD record
- ord-8fe34076fa75497e95996cd165b7e016
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683070B2
Reaction notes
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