HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 1,2-Benzenediol, 4-(2-nitroethenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Product | 1,2-Benzenediol, 4-(2-nitroethenyl)- | HCID 5487258 | 61% |
Reaction Steps
Ammonium acetate (5.6 g, 72.73 mmol, 1.00 equiv) was added to a solution of 3,4-dihydroxybenzaldehyde (10 g, 72.41 mmol, 1.00 equiv) and nitromethane (50 mL). The resulting mixture was heated at reflux for about 16 hours, and then concentrated in vacuo. The resulting residue was then purified by silica gel column chromotagraphy (ethyl acetate/petroleum ether (1:5)) to give the title compound as a yellow oil (8 g, yield=61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524733B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-948b2595e32c48ddb6b3bc450387cff4 |
| Source note | uspto-grants-2013_09 |