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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73438Generated: October 30, 2026

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

https://huagongshe.com/reaction/73438

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, 6.4, 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 numberUS08829052B2
Source datasetuspto-grants-2014_09
ORD IDord-c0ad74dc048c474eb8e1d7fded1c7b12
Source noteuspto-grants-2014_09