Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495372Generated: October 25, 2026

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

https://huagongshe.com/reaction/495372

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 1-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939872B2
Source datasetuspto-grants-2005_09
ORD IDord-d69b87f4c03c41eb9db78e5e4ada6c17
Source noteuspto-grants-2005_09