HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyethylamine → 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobenzenesulfonyl fluoride | HCID 66823 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide | HCID 16781918 | 65.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855719B1 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-f9f01c43aca840369211d72fc8d690c8 |
| Source note | uspto-grants-2005_02 |