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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251705Generated: October 26, 2026

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

https://huagongshe.com/reaction/2251705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
ReactantAcetyl-5-aminosalicylic acidHCID 13140652—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product2-Ethanoyloxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 997982753%

Reaction Steps

According to the similar procedure in Synthesis Example 1, by using 2-ethanoyloxy-5-aminobenzoic acid (0.81 g, 4.10 mmole) which was prepared from Synthesis Example (14-3), DMF (15 ml), TEA (0.1 ml), tetrabutyl ammonium iodide (5 mg), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (1.02 ml, 6.15 mmole), 0.92 g (53.0% yield) of was obtained 2-ethanoyloxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319160B2
Source datasetuspto-grants-2008_01
ORD IDord-8be40591d7d94d4eaf036d6695166cd9
Source noteuspto-grants-2008_01