HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3,4,5-Trimethoxy-2-nitrophenyl)methanol → 3,4,5-Trimethoxy-2-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3,4,5-Trimethoxy-2-nitrophenyl)methanol | HCID 227988 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4,5-Trimethoxy-2-nitrobenzaldehyde | HCID 18697918 | 30% |
Reaction Steps
Active manganese dioxide (8.0 g) was added to a solution of 3,4,5-trimethoxy-2-nitrobenzyl alcohol (1.01 g, 4.15 mmol), prepared in the step (a), in methylene chloride (15 ml), and the mixture was stirred at room temperature overnight. Further, active manganese dioxide (8.0 g) was added thereto, and the mixture was stirred at room temperature for 8 hr. The reaction mixture was filtered through Celite, and the solvent was removed under reduced pressure to give 3,4,5-trimethoxy-2-nitrobenzaldehyde (300 mg, 30%) as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093714 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-ef5325f9ec414c1bb60e57b17cff8077 |
| Source note | uspto-grants-2000_07 |