Hydrochloric Acid → HCID 67970562, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:13]([F:15])[F:14])=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9])#[N:2].[ClH:16].[H][H]>[Pd].CO>[ClH:16].[NH2:2][CH2:1][C:3]1[CH:4]=[CH:5][C:6]([CH:13]([F:14])[F:15])=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Purge a mixture of methyl 5-cyano-2-(difluoromethyl)benzoate (9.37 g, 44.4 mmol, 1.0 equiv), palladium (10% on carbon, 3.00 g, 2.82 mmol, 0.064 equiv), and MeOH (50 mL) with nitrogen; then add hydrochloric acid (37 wt % aqueous, 8.0 mL, 105.6 mmol, 2.38 equiv); and stir the resulting suspension under 275 kPag of hydrogen at room temperature overnight. Remove the solids by filtration; concentrate the filtrate under reduced pressure; and dry the resulting material in a 40° C. vacuum oven overnight to give the title compound as a light brown solid (7.01 g, 83% yield). ES/MS (m/z) 216 (M+1).
Workup
- customPurge
- customRemove the solids
- filtrationby filtration
- concentrationconcentrate the filtrate under reduced pressure
- customand dry the resulting material in a 40° C. vacuum oven overnight
Sources & evidence
- ORD record
- ord-072d06f217394903b25797486c687845
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08648200B2
Reaction notes
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