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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251695Generated: November 1, 2026

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

https://huagongshe.com/reaction/2251695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
Reactant5-Amino-2-bromobenzoic acidHCID 2769624—
SolventDimethylformamideHCID 6228—
Product2-Bromo-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 1045619476.9%

Reaction Steps

According to the similar procedure in Synthesis Example 1, by using 5-amino-2-bromobenzoic acid (1.05 g, 6.12 mmole) which was prepared from Synthesis Example (4-1), DMF (50 ml) and 2,3,5,6-tetrafluoro-4-trifloromethylbenzyl bromide (1.16 g, 6.99 mmole), 2.02 g (76.9% yield) of 2-bromo-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid was obtained as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319160B2
Source datasetuspto-grants-2008_01
ORD IDord-89d8f042929d4e13a3aa99aca12ade14
Source noteuspto-grants-2008_01