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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787885Generated: November 1, 2026

4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide → HCID 10028645, compound

https://huagongshe.com/reaction/1787885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
ReactantHCID 22341904HCID 22341904—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 10028645HCID 1002864549%

Reaction Steps

According to the similar procedure in Synthesis Example (14-4), by using 5-amino-2-cyclohexanecarbonyloxybenzoic acid (1.03 g, 3.95 mmole) which was prepared from Synthesis Example (16-2), DMF (15 ml), TEA (0.10 ml), tetrabutyl ammonium iodide (10 mg), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (1.01 ml, 5.92 mmole), 0.95 g (49.0% yield) of was obtained 2-cyclohexanecarbonyloxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511074B2
Source datasetuspto-grants-2009_03
ORD IDord-ae901311a46d4e2eb7b0e3a82f66843e
Source noteuspto-grants-2009_03