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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565001Generated: October 30, 2026

Sodium Trifluoroacetate → 3-Benzyloxy-6-trifluoromethyl-2-nitrotoluene

https://huagongshe.com/reaction/565001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium TrifluoroacetateHCID 517019—
ReactantHCID 21194170HCID 21194170—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Benzyloxy-6-trifluoromethyl-2-nitrotolueneHCID 10543034—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1.50 g (4.66 mmol) of 3-benzyloxy-6-bromo-2-nitrotoluene, 6.33 g (46.6 mmol) of sodium trifluoroacetate, 4.43 g (23.3 mmol) of copper (I) iodide and 80 ml of N-methylpyrrolidone was heated at 160° C. for 7 hours while stirring. Next, the solvent was distilled off under reduced pressure and ethyl acetate was added to the resulting residue. Insoluble matters were then filtered off. The filtrate was washed twice with water. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was isolated and purified by silica gel column chromatography to give 0.70 (48.3%) of 3-benzyloxy-6-trifluoromethyl-2-nitrotoluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-a7e9e7777e194a9b98249cb919663a5e
Source noteuspto-grants-2001_01