HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Chloromethyl)benzoyl chloride → HCID 22291067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Chloromethyl)benzoyl chloride | HCID 70136 | — |
| Reactant | N-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamide | HCID 11529455 | — |
| Product | HCID 22291067 | HCID 22291067 | 94% |
Reaction Steps
Using an analogous procedure to that described in Example 37, 4-chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)-3-trifluoromethylbenzamide to give the title compound in 94% yield; NMR Spectrum: (DMSOd6) 2.21 (s, 3H), 4.84 (s, 2H), 7.25 (d, 1H), 7.57 (m, 3H), 7.76 (t, 1H), 7.83 (d, 1H), 7.96 (m, 3H), 8.26 (m, 2H), 9.92 (s, 1H), 10.44 (s, 1H); Mass Spectrum: M−H− 445.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06579872B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-0019b730bbda42398002df401c749785 |
| Source note | uspto-grants-2003_06 |