HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884262Generated: October 27, 2026
Sodium Hydroxide → 3-Methoxy-4-phenylmethoxyphenylisopropylamine
https://huagongshe.com/reaction/1884262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1-Benzyloxy-2-methoxy-4-(2-nitropropenyl)benzene | HCID 53422134 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methoxy-4-phenylmethoxyphenylisopropylamine | HCID 14579452 | 93.9% |
Reaction Steps
To a mixture of 1.03 g (27.1 mmol) of lithium aluminum hydride and 20 ml of anhydrous tetrahydrofuran, an anhydrous tetrahydrofuran solution of 2.70 g (9.03 mmol) of 1-benzyloxy-2-methoxy-4-(2-nitropropenyl)benzene was added dropwise under vigorous stirring over about 90 minutes and refluxed for 2 hours by heating. The reaction mixture was cooled and aqueous sodium hydroxide solution was added thereto. After the precipitates were filtered off with celite-precoated glass filter, the solvent was distilled off from the filtrate under reduced pressure. The residue was extracted with ethyl acetate, washed with saturated brine, dried over potassium carbonate and the solvent was distilled off under reduced pressure to give 2.30 g of crude 2-(4-benzyloxy-3-methoxyphenyl)-1-methylethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762321B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-06d620cfac2d4d7795258987f215d516 |
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| Source note | uspto-grants-2004_07 |
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