Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 15166210 | HCID 15166210 | — |
| Product | HCID 19600572 | HCID 19600572 | — |
Reaction Steps
15 ml of acetic anhydride was added to 25 g of 4-(2-hydroxyethoxy)-2,3-dimethylpyridine N-oxide to obtain a solution. This solution was stirred at 90° C. for 2 hours, followed by the addition of ethanol. The obtained mixture was distilled under a reduced pressure to obtain 4-(2-acetoxyethoxy)-2-acetoxymethyl-3-methylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05045552 |
|---|
| Source dataset | uspto-grants-1991_09 |
|---|
| ORD ID | ord-3e321e6a39d84071b09d24e5ffd3a732 |
|---|
| Source note | uspto-grants-1991_09 |
|---|
