HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Acetoxymethyl-4-acetylaminopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 178428516 | HCID 178428516 | — |
| Product | 2-Acetoxymethyl-4-acetylaminopyridine | HCID 19913003 | — |
Reaction Steps
6.5 g of the thus obtained 2-methyl-4-aminopyridine-N-oxide were dissolved in 80 ml of acetic anhydride and heated for 3 hours at 80° to 100° C. The excess anhydride was decomposed with ice, the solution adjusted with Na2CO3 to pH 8 and extracted with dichloromethane. After rotating in the organic phase, 5 g of 2-acetoxymethyl-4-acetylaminopyridine were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997835 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-ff9e7a6232b0456fa2dc9fdc9ec28feb |
| Source note | uspto-grants-1991_03 |