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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967889Generated: October 25, 2026

3-(Chloromethyl)benzoyl chloride → N-[5-(3-trifluoromethylbenzamido)-2-methylphenyl]-3-(chloromethyl)benzamide

https://huagongshe.com/reaction/967889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)benzoyl chlorideHCID 2733324—
ReactantN-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 11529455—
ProductN-[5-(3-trifluoromethylbenzamido)-2-methylphenyl]-3-(chloromethyl)benzamideHCID 2229101794%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956037B2
Source datasetuspto-grants-2005_10
ORD IDord-d72481ac12e242f6a680ca73d830346e
Source noteuspto-grants-2005_10