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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | Diallyl malonate | HCID 228227 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Allyl 7-ethyl 2-allyloxycarbonylheptanedioate | HCID 57831364 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998988B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-7777bea4c03e4d658961c12484818688 |
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| Source note | uspto-grants-2011_08 |
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