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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584863Generated: October 25, 2026

4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide → 2-Methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid

https://huagongshe.com/reaction/584863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
Reactant5-Amino-2-methylbenzoic acidHCID 10374614—
SolventDimethylformamideHCID 6228—
Product2-Methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 1033978727%

Reaction Steps

According to the similar procedure in Synthesis Example 1, by using 5-amino-2-methylbenzoic acid (2.06 g, 15.0 mmole), DMF (60 ml), TEA (4 ml), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (5.52 ml, 17.7 mmole), 1.50 g (27.0% yield) of 2-methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927303B2
Source datasetuspto-grants-2005_08
ORD IDord-2bcb9e9b9bc54c2491a9b2e4ce3954d3
Source noteuspto-grants-2005_08