HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433675Generated: October 25, 2026
Water → N-Methyl-4-benzyloxy-2-methylaniline
https://huagongshe.com/reaction/1433675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1H-Benzotriazole-1-methanol | HCID 224169 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(Benzyloxy)-2-methylaniline | HCID 16773053 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Methyl-4-benzyloxy-2-methylaniline | HCID 22936498 | 62.5% |
Reaction Steps
After dissolving 4-benzyloxy-2-methylaniline (6.55 g, 30.72 mmol) in N,N-dimethylformamide (10 ml) and methanol (60 ml), 1H-benzotriazole-1-methanol (4.58 g, 30.72 mmol) was added and the mixture was stirred for 30 minutes at room temperature. N,N-Dimethylformamide (20 ml) was added for complete dissolution of the precipitated crystals, sodium borohydride (2.32 g, 61.44 mmol) was added in small portions at a time at room temperature (internal temperature increase), and the mixture was stirred for 30 minutes. Water was added to the reaction solution, extraction was performed ethyl acetate, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel and purified by silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (4.364 g, 19.20 mmol, 62.49%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612092B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-0af608dc2b5c4dc7a212587f5adffdc9 |
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| Source note | uspto-grants-2009_11 |
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