HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650980Generated: October 29, 2026
Sodium Hydroxide → 2-[3-Methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethylamine
https://huagongshe.com/reaction/650980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1-[2-Methoxy-4-(2-nitro-vinyl)-phenoxymethyl]-naphthalene | HCID 53870037 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[3-Methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethylamine | HCID 21710157 | — |
Reaction Steps
10 g of lithium aluminium hydride are placed in 200 ml of tetrahydrofuran; the mixture is stirred at room temperature. 25.8 g of 1-[2-methoxy-4-(2-nitro-vinyl)-phenoxymethyl]-naphthalene dissolved in 300 ml of tetrahydrofuran are added dropwise thereto over a period of 90 minutes. The reaction mixture is heated at reflux for 4 hours. After cooling, 40 ml of 1 N sodium hydroxide solution are cautiously added dropwise, external cooling being effected using an ice bath. When the addition is complete, the reaction mixture is stirred, without cooling, for one hour, then filtered with suction over Celite and washed with a small amount of tetrahydrofuran. The filtrate is dried over potassium carbonate and concentrated by evaporation, yielding 2-[3-methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethylamine in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06277849B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-394898bf230a4a36b0d35ae24f7e562b |
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| Source note | uspto-grants-2001_08 |
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