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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482661Generated: November 2, 2026

4-Nitrophenol → 1-[(2-methoxyethoxy)methoxy]-4-nitroBenzene

https://huagongshe.com/reaction/1482661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantDichloromethaneHCID 6344—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantDiisopropylethylamineHCID 81531—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Product1-[(2-methoxyethoxy)methoxy]-4-nitroBenzeneHCID 1960908695.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 50 mL, 3-neck RBF equipped with a magnetic stirrer, reflux condenser, calcium chloride guard tube and thermometer pocket were sequentially charged 4-nitrophenol (1.50 g), DIPEA (2.90 mL) and DCM (25 mL). MEM-Cl (2.016 g) was added drop wise to the reaction at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and then allowed to stir at room temperature for 4 hours. The reaction was monitored on TLC using hexane:ethyl acetate (8:2) as mobile phase. After completion, the reaction was poured into water and the product was extracted in ethyl acetate and washed with brine. The organic layer was dried over sodium sulfate and the solvent was removed under reduced pressure to give 2.35 g of 1-[(2-methoxyethoxy)methoxy]-4-nitrobenzene as a solid, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415049B2
Source datasetuspto-grants-2016_08
ORD IDord-5c994c2bb51347598683b2fd763a399e
Source noteuspto-grants-2016_08