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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23922Generated: October 25, 2026

2-Methoxyethylamine → 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide

https://huagongshe.com/reaction/23922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
ReactantTriethylamineHCID 8471—
Reactant4-Aminobenzenesulfonyl fluorideHCID 66823—
Solvent1-ButanolHCID 263—
Product4-amino-N-(2-methoxyethyl)benzene-1-sulfonamideHCID 1678191865.4%

Reaction Steps

A mixture of 2-methoxyethylamine (859 mg, 11.4 mmol), sulphanilyl fluoride (1.0 g, 5.71 mmol), and triethylamine (1.72 g, 22.9 mmol) in n-butanol (15 ml) was heated at reflux for 18 hours. The mixture was allowed to cool and the volatiles were removed by evaporation. The residue was purified by chromatography eluting with ethyl acetate/hexane (50:50) increasing in polarity to (70:30) to give the title compound (860 mg, 65%). NMR: 2.78 (q, 2H), 3.15 (s, 3H), 3.25 (t, 2H), 5.87 (s, 2H), 6.58 (d, 2H), 7.10 (t, 1H), 7.40 (d, 2H); m/z: 231 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855719B1
Source datasetuspto-grants-2005_02
ORD IDord-f9f01c43aca840369211d72fc8d690c8
Source noteuspto-grants-2005_02