HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 2-[(2,6-Dichloro-4-methylphenyl)amino]benzoic acid | HCID 18936982 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde | HCID 15027377 | 120.7% |
Reaction Steps
A mixture in dry dichloromethane (135 mL) of 2-[(2,6-dichloro-4-methylphenyl)amino]benzoic acid (meclofenamic acid) (7.0 g, 23.6 mmol), N,O-dimethylhydroxylamine hydrochloride (5.0 g, 51.9 mmol), carbon tetrabromide (17.2 g, 51.9 mmol), triphenylphosphine (13.6 g, 51.9 mmol), and pyridine (10 mL) was stirred at ambient temperature for 48 hours. The reaction mixture was poured into 10% HCl (100 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with water and brine, dried over MgSO4, filtered, and evaporated in vacuo. Purification by chromatography on silica gel (9:1 hexane/ethyl acetate) provided 7.98 g (99%) of 2-[(2,6-dichloro-3-methylphenyl)amino]benzaldehyde as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840758 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-eea4ac23e351495a8deb42c525e825c6 |
| Source note | uspto-grants-1998_11 |