Hydrogen Peroxide → HCID 20475746, compound
Reaction equation
[OH:1]O.[C:3]1([S:9][C:10]2[N:15]=[CH:14][C:13]([Cl:16])=[CH:12][N:11]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)(=O)C>[C:3]1([S:9]([C:10]2[N:15]=[CH:14][C:13]([Cl:16])=[CH:12][N:11]=2)=[O:1])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
30% hydrogen peroxide solution (0.8 g) was added to a solution of 2-phenylthio-5-chloropyrimidine (5 mmol) in acetic acid (4 ml) and left at room temperature for 60 h). The solution was then diluted (25 ml) and the precipitate purified by thick-layer (2 mm) chromatography on silica gel 60F (Merck). The plates were developed with EtOAc; yield 50% m.p. 115° C. (ligroin). 1H NMR (CDCl3): δ7.4 and 7.8 (Ph), 8.71 (H-4, H-6).
Workup
- additionThe solution was then diluted (25 ml)
- customthe precipitate purified by thick-layer (2 mm) chromatography on silica gel 60F (Merck)
Sources & evidence
- ORD record
- ord-36370c2d98234935b98faee019f07cd7
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04423047
Reaction notes
Loading…