HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1H-Indole-6-carbaldehyde O-methyl-oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 1H-Indole-6-carboxaldehyde | HCID 2773435 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-Indole-6-carbaldehyde O-methyl-oxime | HCID 72250860 | 82.6% |
Reaction Steps
An amount of 1H-Indole-6-carbaldehyde (50 mg, 0.34 mmol) is added to pyridine (2.0 ml) at room temperature, followed by addition of methoxylamine hydrogen chloride (31.6 mg, 0.38 mmol). The mixture is stirred at ambient temperature for 24 h, and 10 mL of water is added. After the solvents were evaporated, the residue is dissolved 10 mL of anhydrous ether, washed successively with 10 mL of aqueous sodium bicarbonate, 10 mL of sodium bisulfite, and 10 mL of brine. Dried over magnesium sulfate, evaporated to give a white solid (49 mg, 0.281 mmol). MS (ESI) m/z 176.3 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-9755bd7b0d8e47f39496ab019f24d438 |
| Source note | uspto-grants-2010_05 |