Hydrochloric Acid → HCID 178488790, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]([CH3:16])=[N:11][C:12](=[O:15])[NH:13][CH:14]=2)=[CH:5][CH:4]=1.[ClH:17].CCOCC>CO>[ClH:17].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[C:10]([CH3:16])=[N:11][C:12](=[O:15])[NH:13][CH:14]=2)=[CH:7][CH:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
3.5 g of 5-(4-methoxyphenyl)-4-methyl-2-(1H)-pyrimidinone are dissolved in methanol, the solution is acidified with ethereal hydrochloric acid (pH 2-3), and ether is added to incipient opalescence. The solution is cooled and the crystals are filtered off with suction. After drying, 3.3 g of 5-(4-methoxyphenyl)-4-methyl-2-(1H)-pyrimidinone hydrochloride are obtained. Melting point 265° C. (decomposition).
Workup
- additionis added to incipient opalescence
- temperatureThe solution is cooled
- filtrationthe crystals are filtered off with suction
- customAfter drying
Sources & evidence
- ORD record
- ord-feecbc3565a14fa8abce4e12d79ec66e
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04582834
Reaction notes
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