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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584872Generated: October 29, 2026

4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide → HCID 10455841, compound

https://huagongshe.com/reaction/584872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
ReactantHCID 22341900HCID 22341900—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 10455841HCID 1045584151%

Reaction Steps

According to the similar procedure in Synthesis Example 14-4, by using 5-amino-2-propanoyloxybenzoic acid (0.32 g, 1.53 mmole) which was prepared from Synthesis Example (15-2), DMF (10 ml), TEA (0.05 ml), tetrabutyl ammonium iodide (3 mg), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (0.38 ml, 2.30 mmole), 0.34 g (51.0% yield) of was obtained 2-propanoyloxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927303B2
Source datasetuspto-grants-2005_08
ORD IDord-8c43627141d5467b81dabbf591c27c6c
Source noteuspto-grants-2005_08