HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 3,4-Dimethoxy-5-nitrobenzhydrol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3,4-Dimethoxy-5-nitrobenzaldehyde | HCID 10867565 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dimethoxy-5-nitrobenzhydrol | HCID 21458992 | — |
Reaction Steps
25 ml of 2M phenyl lithium solution (in benzene/ether (7:3)) are added dropwise within 15 minutes to 10.0 g of 3,4-dimethoxy-5-nitrobenzaldehyde dissolved in 150 ml of tetrahydrofuran and the mixture is stirred at 0° for 1 hour and at 20° for 2 hours. The mixture is subsequently treated with 150 ml of 2N sulfuric acid and extracted three times with 150 ml of ether. The combined ether phases are washed with sodium chloride solution, dried over sodium sulfate and evaporated. The thus-obtained residue is chromato graphed on 180 g of silica gel with methylene chloride. There is obtained 3,4-dimethoxy-5-nitrobenzhydrol as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389653 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-7f705cc59c854636ad254ff1b942e9c2 |
| Source note | uspto-grants-1995_02 |