HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyaniline → 2-methoxy-N-(2-methoxyethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-methoxy-N-(2-methoxyethyl)aniline | HCID 1589050 | 65% |
Reaction Steps
A suspension of 24.6 g (200 mmol) o-anisidine M10, 20.8 g (220 mmol) chloroethyl methyl ether M11, 30.4 g (220 mmol) K2CO3 and 18.3 g (110 mmol) KI in 110 ml DMF was heated at 95° C. for 24 hours. DMF was evaporated, and the residue was digested with 100 ml CHCl3, filtered, and the precipitate washed with 2×50 ml CHCl3. The solvent was evaporated to give 41.2 g crude oil. This oil was purified by a plug packed with 184 g silica gel 100 with CHCl3/cyclohexane (1:1, v/v) as eluant, to afford 23.5 g pure product (yield: 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06171866B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2f5d5daa013a4bc1b544cea3c2debd7f |
| Source note | uspto-grants-2001_01 |