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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantSodium AzideHCID 33557—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantDiethyl [3-(3-pyridyl)-propyl]malonateHCID 10468827—
SolventDimethylformamideHCID 6228—
ProductPropanedioic acid, (4-azidobutyl)[3-(3-pyridinyl)propyl]-, diethyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-2856ff07e56d47148332808877fdaa07
Source noteuspto-grants-1991_06