HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607383Generated: October 26, 2026
Diethyl Ether → Diethyl [(naphthalen-1-yl)methyl](4-phenylbutyl)propanedioate
https://huagongshe.com/reaction/1607383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-4-phenylbutane | HCID 259668 | — |
| Reactant | Diethyl (1-naphthyl)methylmalonate | HCID 9972002 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Diethyl [(naphthalen-1-yl)methyl](4-phenylbutyl)propanedioate | HCID 13727089 | 73.4% |
Reaction Steps
To a solution of 2.62 g of 2-(1-naphthylmethyl)malonic acid diethyl ester in 40 ml of dry 1,2-dimethoxyethane was added 0.46 g of a 50% sodium hydride (suspension in oil) while ice-cooling, and then 2.05 g of 4-phenylbutyl bromide was added dropwise to the mixture. The mixture was heated under reflux for 19 hours. After cooling, an aqueous ether was added to the reaction mixture and the mixture was extracted with diethyl ether. The ethereal layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (eluent: benzene/hexane=1/1 by volume) to obtain 2.77 g of 2-(1-naphthylmethyl)-2-(4-phenylbutyl)malonic acid diethyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863904 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-4fbabe065ed44849b7e724776d09729e |
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| Source note | uspto-grants-1989_09 |
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