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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222768Generated: October 25, 2026

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

https://huagongshe.com/reaction/2222768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
Reactant5-Amino-2-methoxybenzoic acidHCID 13549244—
SolventDimethylformamideHCID 6228—
Product2-Methoxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 1004633231.5%

Reaction Steps

According to the similar procedure in Synthesis Example 1, by using 5-amino-2-methoxy-benzoic acid (2.10 g, 12.7 mmole), DMF (50 ml), TEA (6 ml), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (2.00 ml, 14.0 mmole), 1.50 g (31.5% yield) of 2-methoxy-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 numberUS07371896B2
Source datasetuspto-grants-2008_05
ORD IDord-f8476c77d76a47faa4697bbd97f77147
Source noteuspto-grants-2008_05