HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426993Generated: October 26, 2026
Acetic Anhydride → N-(4-Chloropyridin-2-yl)acetamide
https://huagongshe.com/reaction/1426993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Product | N-(4-Chloropyridin-2-yl)acetamide | HCID 22832129 | 99% |
Reaction Steps
Commercially available 2-amino-4-chloropyridine (50 g, 389 mmol) was dissolved in acetic anhydride (500 mL), triethylamine (271 mL, 1.94 mol) was added at 20° C., and the mixture was stirred at 60° C. for 12 hours. The mixture was cooled to 25° C. and then the solvent was evaporated. The residue was purified with silica gel column chromatography (n-heptane:ethyl acetate=4:1-1:1) and then the target fraction was concentrated under vacuum to obtain the title compound (66 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08933099B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-c37ec05972464ce387071ecd9eec2dbb |
|---|
| Source note | uspto-grants-2015_01 |
|---|