HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3,5-Dimethoxy-N-methylbenzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3,5-Dimethoxyaniline | HCID 66301 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Dimethoxy-N-methylbenzenamine | HCID 14523536 | 29.9% |
Reaction Steps
A solution of 3,5-dimethoxyaniline (13.8 g, 90 mmol), Iodomethane (12.7 g, 90 mmol), and sodium acetate (7.4 g, 90 mmol) in 100 ml of anhydrous THF was stirred under nitrogen atmosphere for 10 hr. Then, THF was removed by rotary evaporation. The crude product was partitioned between water and ethyl ether. The ethereal extraction was separated and washed with water, brine, and dried over Na2SO4. Filtration and removal of solvent provided 13.6 g of crude product. The crude product was chromatographed on silica gel (33% acetone-petroleum ether) to afford the expected product 4.5 g (27% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183313B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-0736f5026ca84458909cfdd1c9391405 |
| Source note | uspto-grants-2007_02 |