HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 4-(Benzyloxy)-5-methoxy-2-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Benzyloxy-3-methoxy-benzonitrile | HCID 793771 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(Benzyloxy)-5-methoxy-2-nitrobenzonitrile | HCID 11673618 | — |
Reaction Steps
4-benzyloxy-3-methoxybenzonitrile (4.78 g, 20 mmol) in acetic acid (10 ml) was slowly added to nitric acid (25 ml) at 20° C. to 30° C. The mixture was stirred at room temperature for 6 hours, basified (pH 10-11) with cooling (KOH 10N), extracted with methylene chloride, dried over MgSO4 evaporated. The solid was recristallysed in hot EtOAc, a yellow solid of title compound was obtained (3.62 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919338B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-e617e8aafd544db5975afef715b40ad1 |
| Source note | uspto-grants-2005_07 |