HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-(3,4-Dimethoxy-5-nitrophenyl)-2-pyridinemethanol → 3,4-Dimethoxy-5-nitrophenyl 2-pyridyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-(3,4-Dimethoxy-5-nitrophenyl)-2-pyridinemethanol | HCID 21459111 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,4-Dimethoxy-5-nitrophenyl 2-pyridyl ketone | HCID 17977723 | — |
Reaction Steps
7 g of manganese dioxide and added portionwise to 4.0 g of α-(3,4-dimethoxy-5-nitrophenyl)-2-pyridine-methanol dissolved in 100 ml of acetone while constantly heating under reflux over a period of 2.5 hours. Thereupon, the mixture is heated under reflux for an additional 2 hours. The manganese salts are subsequently filtered and the residue obtained after evaporation is recrystallized from ether/hexane. There is obtained 3,4-dimethoxy-5-nitrophenyl 2-pyridyl ketone of m.p. 113°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633371 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-138571790bae4b9aa8198da6b9657a45 |
| Source note | uspto-grants-1997_05 |