HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494063Generated: October 30, 2026
Sodium Iodide → Propanedioic acid, (4-azidobutyl)[3-(3-pyridinyl)propyl]-, diethyl ester
https://huagongshe.com/reaction/1494063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | Diethyl [3-(3-pyridyl)-propyl]malonate | HCID 10468827 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Propanedioic acid, (4-azidobutyl)[3-(3-pyridinyl)propyl]-, diethyl ester | HCID 10068124 | — |
Reaction Steps
To a solution of 63.34g (0.23 mole) of diethyl [3-(3-pyridyl)-propyl]malonate in 1.1L dimethylformamide is in small portions 9.91 g (0.25 mole) of sodium hydride as a 60% dispension in oil. After stirring at room temperature for 0.5 hours, 28 mL (0.23 mole) of 1-bromo-4-chlorobutane is added and then heated to 60° for 10 hours. Then 68.26 g (0.46 mole) sodium iodide is added followed by 44.44 g (0.68 mole) sodium azide and 9.0 g crown ether 18-Crown-6. The reaction mixture is heated for 15 hours at 60°, is then cooled and poured on ice. The mixture is then extracted with ether (4×500 mL). Combined organic extracts are extracted with 1N aqueous hydrochloric acid (1×200, 2×100 mL). Combined aqueous extract is adjusted to pH 8 by addition of solid sodium bicarbonate and then extracted with ether (3×300 mL). Combined organic extracts are washed with water (3×100 mL), brine (1×300 mL), dried (MgSO4), filtered and then evaporated to dryness to give diethyl [4-azidobutyl][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-2856ff07e56d47148332808877fdaa07 |
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| Source note | uspto-grants-1991_06 |
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