HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Chloromethyl)benzoyl chloride → N-[5-(3-trifluoromethylbenzamido)-2-methylphenyl]-3-(chloromethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | N-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamide | HCID 11529455 | — |
| Product | N-[5-(3-trifluoromethylbenzamido)-2-methylphenyl]-3-(chloromethyl)benzamide | HCID 22291017 | 94% |
Reaction Steps
Using an analogous procedure to that described in Example 37, 3-chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)-3-trifluoromethylbenzamide to give the title compound in 94% yield; NMR Spectrum: (DMSOd6) 2.2 (s, 3H), 4.85 (s, 2H), 7.25 (d, 1H), 7.6 (m, 3H), 7.8 (m, 2H), 7.95 (d, 2H), 8.05 (s, 1H), 8.16 (m, 2H), 9.96 (s, 1H), 10.44 (s, 1H); Mass Spectrum: M−H− 445.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956037B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-d72481ac12e242f6a680ca73d830346e |
| Source note | uspto-grants-2005_10 |