HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 2-Chloro-N-(2-chloro-4-fluoro-6-methylphenyl)-N-(4-methylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-4-fluoro-6-methyl-N-(4-methylphenyl)benzenamine | HCID 57952166 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-N-(2-chloro-4-fluoro-6-methylphenyl)-N-(4-methylphenyl)acetamide | HCID 57952156 | — |
Reaction Steps
1.32 g of N-(2′-Chloro-4′-fluoro-6′-methylphenyl)-4-methylaniline is reacted with chloracetylchloride (1.76 g) at 90° C. for 30 minutes. The cooled mixture is stirred with toluene (20 ml) and aqu. sodium carbonate for 30 minutes and the organic phase is evaporated. The residue is purified flash-chromatography on silica using toluene affording 1.04 g of N-(2′-chloro-4′-fluoro-6′-methylphenyl)-N-chloroacetyl-4-methylaniline as a solid which is recrystallised from heptane/2-propanol (9:1), mp.: 96-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906677B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ec253b70644c48d1956d6436cc69e44a |
| Source note | uspto-grants-2011_03 |