Hydrogen Sulfide → HCID 54052991, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)[C:5]#[N:6].C(N(CC)CC)C.N1C=CC=CC=1.[SH2:26]>O>[CH3:1][O:2][CH2:3][CH:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1)[C:5]([NH2:6])=[S:26]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
Two grams of 3-methoxy-2-(2-pyridyl)propionitrile is dissolved in 1.5 g. of triethylamine and 2 g. of dry pyridine, saturated with hydrogen sulfide. The mixture is heated at 100° C. in a sealed bomb for 15 hours. The mixture is cooled, diluted with water and extracted with ether. The organic phase is dried, the solvent is removed and the residue is recrystallized from benzene-petroleum ether to give 3-methoxy-2-(2-pyridyl)thiopropanamide.
Workup
- temperatureThe mixture is cooled
- extractionextracted with ether
- customThe organic phase is dried
- customthe solvent is removed
- customthe residue is recrystallized from benzene-petroleum ether
Sources & evidence
- ORD record
- ord-b5fb160e32094ce2908587e1905cdc1b
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04001241
Reaction notes
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