Hydrochloric Acid → 2-(Pyrimidin-4-yl)benzoic acid hydrochloride
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=2[C:9]([O:11]C)=[O:10])=[N:3][CH:2]=1.[ClH:17]>C(O)(=O)C>[ClH:17].[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=2[C:9]([OH:11])=[O:10])=[N:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of methyl 2-(pyrimidin-4-yl)benzoate (0.49 g), acetic acid (2.0 mL) and 6 N hydrochloric acid (10 mL) was heated under reflux for 5 hr. The solvent was evaporated under reduced pressure, and the obtained residue was washed with ethyl acetate to give the title compound (0.45 g).
Workup
- temperaturewas heated
- temperatureunder reflux for 5 hr
- customThe solvent was evaporated under reduced pressure
- washthe obtained residue was washed with ethyl acetate
Sources & evidence
- ORD record
- ord-64ad8669fdd7422f8bff69f46dec81c0
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440990B2
Reaction notes
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