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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404726Generated: November 4, 2026

Methyl chlorodifluoroacetate → 1-Tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzene

https://huagongshe.com/reaction/2404726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chlorodifluoroacetateHCID 73935—
ReactantPotassium BromideHCID 253877—
ReactantPotassium FluorideHCID 522689—
Reactant1-Tert-butyl-2-(benzyloxy)-5-bromo-4-nitrobenzeneHCID 57470237—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzeneHCID 5747023867%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 1-tert-butyl-2-(benzyloxy)-5-bromo-4-nitrobenzene (913 mg, 2.5 mmol), KF (291 mg, 5 mmol), KBr (595 mg, 5 mmol), CuI (570 mg, 3 mmol), methyl chlorodifluoroacetate (1.6 mL, 15 mmol) and DMF (5 mL) was stirred at 125° C. in a sealed tube overnight, cooled to room temperature, diluted with water and extracted three times with EtOAc. The combined organic layers were washed with brine and dried over anhydrous MgSO4. After removal of the solvent, the residue was purified by column chromatography (0-5% EtOAc-Hexane) to yield 1-tert-butyl-2-(benzyloxy)-5-(trifluoromethyl)-4-nitrobenzene (591 mg, 67%). 1H NMR (400 MHz, CDCl3) 7.66 (s, 1H), 7.37 (m, 5H), 7.19 (s, 1H), 5.21 (s, 2H), 1.32 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802700B2
Source datasetuspto-grants-2014_08
ORD IDord-d4fa90e16efc4468bdc21e3b30408ff2
Source noteuspto-grants-2014_08