Hydrochloric Acid → HCID 178426633, compound
Reaction equation
[NH2:1][C:2]([NH2:4])=[S:3].[C:5]([CH2:8][C:9](=O)[CH3:10])(=O)[CH3:6].[ClH:12]>C(O)C>[ClH:12].[SH:3][C:2]1[N:4]=[C:9]([CH3:10])[CH:8]=[C:5]([CH3:6])[N:1]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Thiourea (76 g, 1.0 mole) was suspended in a solution of 120 g (1.2 moles) of acetylacetone in 2,500 ml of ethanol. The resulting suspension was mixed with 250 ml of concentrated hydrochloric acid, and then reacted under reflux for 2 hours. After completion of the reaction, the reaction liquid was cooled, whereby beautiful yellow needle-like crystals of 2-mercapto-4,6-dimethyl-pyrimidine hydrochloride were formed. The reaction liquid was allowed to stand for a day to deposit sufficiently the crystals, which were then recovered by filtration and dried to obtain 140 g of 2-mercapto-4,6-dimethyl-pyrimidine hydrochloride in yield of 80 %.
Workup
- customreacted
- temperatureunder reflux for 2 hours
- customAfter completion of the reaction
- customthe reaction liquid
- temperaturewas cooled
Sources & evidence
- ORD record
- ord-70c7c9ddee9d45e4970e7efc2e9f6e55
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03960829
Reaction notes
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