Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | HCID 501202 | HCID 501202 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Sodium tungstate | HCID 26052 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 501201 | HCID 501201 | — |
Reaction Steps
To 10.5 g (0.035 mole) of 2-[(2,6-dichlorophenyl)methylthio]-3-methyl-pyridine-N-oxide (See Example 28 above) dissolved in 100 ml of methanol were added a pinch of sodium tungstate and then dropwise 4.2 ml (0.4 mole) of 50% hydrogen peroxide. The temperature was maintained at 25° C. for four hours, and then a cold solution of NaHSO3 was added slowly to destroy residual H2O2. The solid was filtered and air-dried, having a melting point of 178-181° C., yield 10 g. The elemental analysis for C,H,N; the infrared spectrum, and the NMR spectrum all supported the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06498254B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-5f4646f6a5614b7eacb279d4bbd83beb |
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| Source note | uspto-grants-2002_12 |
|---|