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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823762Generated: November 1, 2026

2-Methoxyethylamine → 2-Amino-5-(4-[2-methoxyethyl]aminophenylsulfonyloxy)nitrobenzene

https://huagongshe.com/reaction/1823762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactant4-Amino-3-nitrophenyl 4-fluorobenzenesulfonateHCID 12018843—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-5-(4-[2-methoxyethyl]aminophenylsulfonyloxy)nitrobenzeneHCID 12018847—

Reaction Conditions

Temperature40 °C

Reaction Steps

15.6 g of 2-amino-5-(4-fluorophenylsulfonyloxy)nitrobenzene were combined with 35 ml methoxyethylamine in 100 ml dioxane in a round bottom flask. The reaction mixture was heated to reflux for 8 hours and then cooled to 40° C. and extracted two times with 250 ml water. Concentrate was solubilized with ethyl acetate and extracted with 2N aqueous HCl and water, the organic phase was then dried under reduced pressure, yielding 19.2 g of 2-amino-5-(4-[2-methoxyethyl]aminophenylsulfonyloxy)nitrobenzene (melting point 105° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041668B2
Source datasetuspto-grants-2006_05
ORD IDord-9c2c1c3f2c8a48109c5a6af8e6185440
Source noteuspto-grants-2006_05