Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 67852818 | HCID 67852818 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19756108 | HCID 19756108 | 100% |
Reaction Steps
An amount 40 ml of acetic anhydride was stirred at about 115° C. and a solution of 5.50 g of 6-hexyloxy-α-picoline N-oxide in 20 ml of glacial acetic acid was dropwise added over about one hour. After the dropwise addition, the mixture was stirred at 130° C. for 5 hours, acetic acid and acetic anhydride were removed by concentration under a reduced pressure, the reaction mixture was dissolved in ether, and the remaining acetic acid was neutralized with a sodium hydrogen carbonate solution. After extraction with ether and concentration under a reduced pressure, the residue was separated by silica gel column chromatography (ethyl acetate:hexane=1:9) to give 6.85 g of the desired product (yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05219847 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-5dc1b7c46b8b480eb6564f0bff5939bd |
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| Source note | uspto-grants-1993_06 |
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