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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532170Generated: October 25, 2026

2,2,2-Trifluoroethanol → 1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene

https://huagongshe.com/reaction/532170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantCesium carbonateHCID 10796—
ReactantEthyl 2-oxocyclohexanecarboxylateHCID 95543—
ReactantBenzene, 1,3-dichloro-2-iodo-5-nitro-HCID 112948—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzeneHCID 1385222726.4%

Reaction Steps

A Mixture of Cs2CO3 (17.22 g, 52.84 mmol), CuBr (361 mg, 2.52 mmol) and ethyl 2-oxocyclohexanecarboxylate (856 mg, 5.03 mmol) in DMSO (30 mL) under N2 was stirred for 0.5 h at rt. Then a solution of 1,3-dichloro-2-iodo-5-nitrobenzene (8.0 g, 25.16 mmol) and 2,2,2-trifluoroethanol (3.02 g, 30.19 mmol) in DMSO (20 mL) was added to it. The reaction mixture was stirred at 80° C. for 18 h and cooled to room temperature, and then directly passed through celite. After rinsed with 250 ml of EA, the combined filter was washed by brine, dried over anhydrous Na2SO4, concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (100:1) to provide 1,3-dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene (1.93 g, yield 12.6%) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853186B2
Source datasetuspto-grants-2014_10
ORD IDord-c2c96e8aeee44567aec83a1e90f1aa1b
Source noteuspto-grants-2014_10