Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-4-phenylbutaneHCID 259668—
ReactantDiethyl (1-naphthyl)methylmalonateHCID 9972002—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductDiethyl [(naphthalen-1-yl)methyl](4-phenylbutyl)propanedioateHCID 1372708973.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863904
Source datasetuspto-grants-1989_09
ORD IDord-4fbabe065ed44849b7e724776d09729e
Source noteuspto-grants-1989_09