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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787870Generated: October 27, 2026

5-Amino-2-chlorobenzoic acid → 2-Chloro-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid

https://huagongshe.com/reaction/1787870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-chlorobenzoic acidHCID 37879—
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 997841985.5%

Reaction Steps

According to the similar procedure in Synthesis Example 1, by using 5-amino-2-chlorobenzoic acid (1.02 g, 5.94 mmole) (ACROS, 32525-5000), DMF (50 ml) and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (1.16 g, 6.99 mmole), 2.04 g (85.5% yield) of 2-chloro-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino) benzoic acid was obtained as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511074B2
Source datasetuspto-grants-2009_03
ORD IDord-c222045ee2aa408eb0a418c65a946bf8
Source noteuspto-grants-2009_03