HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494062Generated: October 26, 2026
Diethyl Malonate → Diethyl [3-(3-pyridyl)-propyl]malonate
https://huagongshe.com/reaction/1494062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-(3-Bromopropyl)pyridine hydrobromide | HCID 12701569 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl [3-(3-pyridyl)-propyl]malonate | HCID 10468827 | — |
Reaction Steps
To a solution of 48 mL (0.37 mole) of diethyl malonate in 960 mL ethanol is added 14.03 g (0.61 mole) sodium metal and the mixture is stirred until all of the metal dissolved. The solution is heated to reflux and a solution of 80.04 g (0.28 mole) of 3-(3-pyridyl)-propyl bromide hydrobromide in 960 mL ethanol is added rapidly and the mixture is maintained at reflux for 10 hours. The reaction mixture is evaporated and the residue is taken up in 400 mL of 1N aqueous hydrochloric acid and washed with 400 mL hexane. The aqueous phase is adjusted to pH 8 using solid sodium bicarbonate. The mixture is then extracted with methylene chloride (3×200 mL). Combined organic extracts are dried (MgSO4), filtered and evaporated to dryness to give diethyl [3-(3-pyridyl)-propyl]-malonate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025025 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-d679882bf6634677a11492f3bc56fc09 |
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| Source note | uspto-grants-1991_06 |
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