Hydrochloric Acid → HCID 68681623, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH:7]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=2)[OH:8])=[CH:3][CH:2]=1.[ClH:19]>C(OCC)(=O)C>[ClH:19].[N:1]1[CH:2]=[CH:3][C:4]([CH:7]([C:9]2[CH:14]=[CH:13][C:12]([C:15]([F:16])([F:17])[F:18])=[CH:11][CH:10]=2)[OH:8])=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 21.2 grams (0.070 mole) of 4-pyridyl[4-(trifluoromethyl)phenyl]methanol in 500 mL of ethyl acetate was stirred vigorously and anhydrous hydrogen chloride gas was slowly added during a 15 minute period, below the surface of the solution. The reaction mixture was then stirred for an additional 15 minutes, and a solid was collected by filtration. The solid was washed with ethyl acetate and dried, yielding 11.4 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Workup
- filtrationa solid was collected by filtration
- washThe solid was washed with ethyl acetate
- customdried
Sources & evidence
- ORD record
- ord-100f368f1d82437cabd15e8b53886cef
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683070B2
Reaction notes
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