HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzaldehyde | HCID 68255 | — |
| Reactant | 2,6-Dichloro-3-nitrophenylacetic acid | HCID 54265437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamide | HCID 59833882 | 88.6% |
Reaction Steps
A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (0.90 g, 3.35 mmol) in thionyl chloride (15 mL) is refluxed for one hour. The solvent is removed by concentration and dry toluene is added to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (30 mL) is added (drop-wise) a solution of 2-aminobenzaldehyde (0.365 g, 3.02 mmol) in dichloromethane (5.0 mL). The mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with EtOAc and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product (0.94 g, 88.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449582B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-85921cc9266e4e75939cb8df0dbc30ea |
| Source note | uspto-grants-2008_11 |