Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405616Generated: November 1, 2026

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

https://huagongshe.com/reaction/2405616

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 numberUS08808742B2
Source datasetuspto-grants-2014_08
ORD IDord-cb7cc9aaa1a9423aa8ae6dcd17fac2f8
Source noteuspto-grants-2014_08