HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-Hydroxyiminomethyl-2-methylnitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Nitro-p-tolualdehyde | HCID 1798998 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Hydroxyiminomethyl-2-methylnitrobenzene | HCID 53628318 | 84.6% |
Reaction Steps
To a mixture of 3.00 g of 4-methyl-3-nitrobenzaldehyde, 1.64 g of hydroxylamine hydrochloride, 30 ml of ethanol and 15 ml of water was added 2.24 g of sodium acetate at room temperature, followed by stirring at room temperature for 1 hour. The reaction mixture was added to water, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain 2.77 g of 5-hydroxyiminomethyl-2-methylnitrobenzene. 5-Hydroxyiminomethyl-2-methylnitrobenzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507514B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-eefeb4d668b94d44be720affa48c8b7f |
| Source note | uspto-grants-2013_08 |