HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329522Generated: October 30, 2026
Diethyl Malonate → HCID 15097258, compound
https://huagongshe.com/reaction/329522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-Bromo-5-(2-methoxyethoxy)methoxypentane | HCID 15097257 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15097258 | HCID 15097258 | — |
Reaction Steps
A solution of 37.80 of diethyl malonate dissolved in 20 ml of absolute ethanol was added dropwise to a solution of sodium ethoxide prepared by gradually adding 3.00 g of metallic sodium to 30 ml of absolute ethanol. To the mixture was added a solution of 30.01 g of 1-bromo-5-(2-methoxyethoxy)methoxypentane (prepared as described in Preparation 60) dissolved in 10 ml of absolute ethanol. The mixture was heated under reflux for 21 hours, after which it was allowed to cool, and then the solvent was distilled off. The residue was mixed with water, and the mixture was extracted three times with ethyl acetate. The combined extracts were washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 850 g of silica gel, and 32.78 g of the title compound were obtained, as a colorless oil, from those fractions eluted with a 4:1 by volume mixture of hexane and ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04891363 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-9c188e9f828645758836b8d617beb312 |
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| Source note | uspto-grants-1990_01 |
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