HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21405359, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Dibromomethyl)-5-nitropyridine-3-carboxamide | HCID 21405373 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 21405359 | HCID 21405359 | — |
Reaction Steps
A mixture of 0.48 g of 2-dibromomethyl-5-nitronicotinamide and acetic anhydride was stirred with 3 drops of conc. sulfuric acid at room temperature for 1 hour. The reaction mixture was poured into ice-water, made alkaline with 5% sodium bicarbonate and extracted with ethyl acetate. The extract was dried and the solvent was distilled off to give 0.35 g of crystalline substance, which was then recrystallized from ethyl acetate-n-hexane to give the desired product as yellow needles. mp 168° C. (with decomp.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053608 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-9a7dd89c78c74c27ae18c0ba228f56fb |
| Source note | uspto-grants-1977_10 |