Hydrochloric Acid → HCID 14461104, compound
Reaction equation
[CH2:1]([S:8][C:9]1[N:13]([CH3:14])[N:12]=[C:11]([CH3:15])[C:10]=1C(OCC)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>O>[CH2:1]([S:8][C:9]1[N:13]([CH3:14])[N:12]=[C:11]([CH3:15])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2.0 g of ethyl 5-benzylthio-1,3-dimethylpyrazole-4-carboxylate, 9 ml of concentrated hydrochloric acid and 6 ml of water is refluxed for 11 hours. The reaction mixture is cooled to room temperature, extracted with chloroform. The extract is washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate. Chloroform is evaporated under reduced pressure to yield 1.5 g of the title compound as a colorless oil.
Workup
- temperatureis refluxed for 11 hours
- extractionextracted with chloroform
- washThe extract is washed with a saturated aqueous sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- customChloroform is evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-452715fb2c0b45dca4c28aa472e20e1a
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04872901
Reaction notes
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