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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424019Generated: October 29, 2026

2-Methoxyethanol → 1,2,3-Trifluoro-5-(2-methoxyethoxy)-4-nitrobenzene

https://huagongshe.com/reaction/424019

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant3,4,5-Trifluoro-2-nitrophenolHCID 53880990—
SolventTetrahydrofuranHCID 8028—
Product1,2,3-Trifluoro-5-(2-methoxyethoxy)-4-nitrobenzeneHCID 59386372—

Reaction Steps

To a mixture of 3,4,5-trifluoro-2-nitrophenol (1.93, 10 mmol), Ph3P (3.93 g, 15 mmol), and 2-methoxy-ethanol (1.18 ml, 15 mmol) in anhydrous THF (25 ml) a solution of diisopropyl azodicarboxylate (2.91 ml, 15 mmol) in THF (5 ml) was added at 0° C. and the reaction mixture was stirred at room temperature for 16 h. The volatiles were evaporated and the residue was dissolved in CH2Cl2 (100 ml) and the organic layer was washed with water (100 ml), brine (100 ml) dried (MgSO4) and evaporated. The residue obtained was purified over flash silica gel chromatography to obtain the titled product in 68% (1.70 g) yield. 1H NMR (300 MHz, CDCl3): δ 6.78 (ddd, J=2.4, 6.0, 11.7 Hz, 1H), 4.19 (t, J=4.5 Hz, 2H), 3.72 (t, J=4.5 Hz, 2H), 3.39 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101799B2
Source datasetuspto-grants-2012_01
ORD IDord-6dd7e524dda14ad895eda51b6fa5c964
Source noteuspto-grants-2012_01