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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672671Generated: October 26, 2026

Sodium hydride → 1-Allyl 7-ethyl 2-allyloxycarbonylheptanedioate

https://huagongshe.com/reaction/1672671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 5-bromovalerateHCID 84580—
ReactantDiallyl malonateHCID 228227—
Solvent1,4-DioxaneHCID 31275—
Product1-Allyl 7-ethyl 2-allyloxycarbonylheptanedioateHCID 57831364—

Reaction Conditions

Temperature40 °C

Reaction Steps

16.29 g (407.19 mmol) of sodium hydride are added in portions to a solution of 100 g (542.92 mmol) of diallyl malonate in 900 ml of dry dioxane at 5° C. After gas evolution ceases, the reaction mixture is warmed to 40° C. and stirred for 30 min. Then 56.76 g (271.46 mmol) of ethyl 5-bromovalerate in 100 ml of dry dioxane are added dropwise, and the mixture is stirred at 110° C. for 12 hours. After the reaction is complete, the mixture is cooled to room temperature and added to about 400 ml of ice-water. After neutralization of the reaction mixture with 1 N hydrochloric acid, the organic phase is separated off, and the aqueous phase is extracted three times with 250 ml of ethyl acetate each time. After the organic phases have been combined they are washed with saturated sodium chloride solution and dried over sodium sulfate. After filtration, the reaction solution is concentrated in vacuo. Subsequently excess diallyl malonate is removed by high vacuum distillation (boiling point: 57° C., 0.074 mbar). The distillation residue is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 2:1). 73.92 g (236.65 mmol, 44% of theory) of a colorless liquid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-7777bea4c03e4d658961c12484818688
Source noteuspto-grants-2011_08