HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2921Generated: October 29, 2026
Water → N-methyl-2,6-dimethoxy-4-methylaniline
https://huagongshe.com/reaction/2921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18936468 | HCID 18936468 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-methyl-2,6-dimethoxy-4-methylaniline | HCID 18936485 | 85% |
Reaction Steps
6 g of N-formyl-2,6-dimethoxy-4-methylaniline are suspended in 100 ml of tetrahydrofuran and then 33 ml of a 1M solution of lithium aluminium hydride in tetrahydrofuran are added dropwise under an inert atmosphere. The reaction mixture become homogeneous. The reaction mixture is left at room temperature for 2 hours and then, after cooling to 0° C., 1 ml of water, then 1 ml of a 15% aqueous sodium hydroxide solution and then 3 ml of water are successively added dropwise to the reaction mixture. The whole mixture is diluted with 100 ml of ethyl acetate and the precipitate is filtered. The filtrate, evaporated to dryness, leaves an oily residue which is purified by flash chromatography on a column of silica gel, eluent: toluene/ethyl acetate 8/2 (v/v) in order to obtain N-methyl-2,6-dimethoxy-4-methylaniline in the form of an oil, Yield: 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731340 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-50d4e1528b5f4200af2c175551ee6a2e |
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| Source note | uspto-grants-1998_03 |
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