HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271265Generated: November 1, 2026
Acetic Acid → 5-(Benzyloxy)-2-(methoxycarbonyl)-1-tetralone
https://huagongshe.com/reaction/1271265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10586915 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(Benzyloxy)-2-(methoxycarbonyl)-1-tetralone | HCID 22932001 | 98.2% |
Reaction Steps
Under an argon atmosphere, 2.09 g of 60% sodium hydride was suspended in 30 ml of anhydrous dioxane and 11.51 g of dimethyl carbonate was added. While stirring with heating in an oil bath at 80 to 85° C., a solution of 6.58 g of 5-(benzyloxy)-1-tetralone in 15 ml of dioxane was added dropwise over about one hour. After stirring for one hour, the reaction solution was ice-cooled and 52 ml of an aqueous 1N acetic acid solution was added dropwise. The reaction solution was diluted with water, extracted with diethyl ether, washed with water 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 7.95 g of the desired compound as a pale yellow oily substance.
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-435f2a26a0204e24ab77c276ef29e0fd |
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| Source note | uspto-grants-2007_04 |
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