HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271268Generated: November 3, 2026
Sodium Hydroxide → 5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene
https://huagongshe.com/reaction/1271268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(Benzyloxy)-2-(methoxycarbonyl)-3,4-dihydronaphthalene | HCID 22932012 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisobutylaluminumhydride | HCID 21225700 | — |
| Product | 5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene | HCID 22932021 | 89.1% |
Reaction Steps
Under an argon atmosphere, to a solution of 2.79 g of 5-(benzyloxy)-2-(methoxycarbonyl)-3,4-dihydronaphthalene in 30 ml of dry dichloromethane, 24 ml of diisobutylaluminum hydride (1M toluene solution) was added dropwise at −70° C. or lower, followed by stirring for 20 minutes. To the reaction solution, 26 ml of an aqueous 10% sodium hydroxide solution was added dropwise and, after heating to room temperature, the mixture was extracted with diethyl ether. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 2.25 g of the desired compound as a colorless crystal having a melting point of 59 to 61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205302B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-058514802e3b4bd8aa1af909efe752e8 |
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| Source note | uspto-grants-2007_04 |
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