Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | HCID 12673488 | HCID 12673488 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23335425 | HCID 23335425 | — |
Reaction Steps
A solution of 68 g of 3-(3-methoxyphenoxy)pyridine in 100 ml of glacial acetic acid is treated with 75 g of 40% peracetic acid in acetic acid. The mixture is stirred 16 hours at 35° C. and then is refluxed 1 hour. The mixture is cooled, 100 ml isopropanol added, and the mixture is concentrated at reduced pressure. The oily residue is dissolved in 500 ml of dichloromethane and is washed with excess cold 25% sodium hydroxide solution. The organic layer is concentrated to yield 3-(3-methoxyphenoxy)pyridine 1-oxide, mp 75°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04187379 |
|---|
| Source dataset | uspto-grants-1980_02 |
|---|
| ORD ID | ord-3451cc59b41f4d2eafafb195c3fcf2a8 |
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| Source note | uspto-grants-1980_02 |
|---|
