Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | HCID 12202653 | HCID 12202653 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 12202658 | HCID 12202658 | — |
Reaction Steps
A solution of 110 g of 3-(m-chlorophenoxy)pyridine [Agr. Biol. Chem., 34, 68 (1970)] at 35° C. in 125 ml of glacial acetic acid is treated with 112 g of 40% peracetic acid in acetic acid in four equal portions. The mixture is held at 27° C. for 16 hours and heated at reflux for 1 hour. The mixture is cooled to 70° C., 100 ml of isopropanol is added and the mixture is heated at 95° C. for 1 hour. The warm mixture is concentrated at reduced pressure, dissolved in 500 ml of dichloromethane and extracted with excess 25% sodium hydroxide solution. The dichloromethane is removed at reduced pressure and the 3-(m-chlorophenoxy)pyridine N-oxide is isolated by distillation; 150°-152° C. at 0.15 mm, mp 72°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179563 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-5c2cb0f45dfd4bebbb97bc62e4d3b8dc |
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| Source note | uspto-grants-1979_12 |
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