HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → HCID 54204816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 18962544 | HCID 18962544 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 54204816 | HCID 54204816 | 58.5% |
Reaction Steps
A suspension of 20 g (0.088 mole) of 3,5-dimethoxy-4-hydroxy-2-nitrobenzaldehyde and 21 g (0.27 mole) of dry ammonium acetate in 400 cm3 of acetic anhydride and 15.8 g (0.26 mole) of nitromethane is heated under reflux for 2 hours. The reaction mixture is cooled, then the precipitate is filtered off. After washing with water, recrystallization from an ethanol-water mixture and drying under vacuum, 13.9 g of the desired product is obtained in the form of orangeish-yellow crystals (yield =58% ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05354870 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-46ff00f1f5de47eab778c627a14cd045 |
| Source note | uspto-grants-1994_10 |