HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dinitrobenzaldehyde → (2,6-Dinitrophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dinitrobenzaldehyde | HCID 69073 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2,6-Dinitrophenyl)methanol | HCID 119332 | 75.7% |
Reaction Steps
To a suspension of 2,6-dinitrobenzaldehyde (19.6 g, 0.1 mole) in methanol (200 ml), sodium borohydride (5.8 g) was added in a small portion at 15°-25° C., the resultant mixture was stirred at room temperature for 1 hour and then concentrated. To the residue, H2O (100 ml) and chloroform (100 ml) were added, followed to by stirring for 1 hour, the chloroform layer was separated, washed with H2O, dried over anhydrous MgSO4 and evaporated to afford 15.0 g of 2,6-dinitrobenzyl alcohol as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05350660 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-224b5304348e4e62893f9c74f5d681ae |
| Source note | uspto-grants-1994_09 |