HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 2-Benzyloxy-3,4-dimethoxybenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(Benzyloxy)-3,4-dimethoxybenzaldehyde | HCID 819579 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Benzyloxy-3,4-dimethoxybenzonitrile | HCID 18470611 | — |
Reaction Steps
A slurry of sodium acetate (17.06 g, 0.208 mol) and hydroxylamine (14.45 g, 0.208 mol) in glacial acetic acid (120 ml) was added to 2-benzyloxy-3,4-dimethoxybenzaldehyde (28.3 g, 0.104 mol) and the resulting suspension stirred at reflux for 18 hours. On cooling, water (250 ml) was added and the mixture extracted with dichloromethane (500 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated under reduced pressure. The crude product was purified on silica gel eluting with hexane:ethyl acetate (80:20 v/v) to give the subtitle compound as an oil that crystallised on standing (21.06 g, 75%). Rf 0.52 (ethyl acetate:hexane, 1:1, v/v). MS m/z 270 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048864 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-5ff4dca0f4d145a982394eb6cbe6f53e |
| Source note | uspto-grants-2000_04 |