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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585537Generated: October 26, 2026

Water → 2-(3-Cyanopropyl)-1,3-dioxolane

https://huagongshe.com/reaction/585537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantSodium CyanideHCID 8929—
Reactant2-(3-Chloropropyl)-1,3-dioxolaneHCID 552072—
SolventDimethylformamideHCID 6228—
Product2-(3-Cyanopropyl)-1,3-dioxolaneHCID 1468402976%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-(3-chloropropyl)-1,3-dioxolane (15.88 g; 0.1054 moles), sodium cyanide (6.46 g; 0.132 moles) and sodium iodide (1.57 g; 0.0105 moles) in DMF (100 mL) was heated at 80° C., with magnetic stirring, under a nitrogen atmosphere for 15 hours. The mixture was allowed to cool, added to water (300 mL) and extracted with ethyl acetate (3×200 mL). The combined extracts were washed with water (200 mL) and saturated aqueous sodium chloride solution (100 mL) and then dried over sodium sulfate. Filtration and evaporation of solvent gave a crude yellow oil which was purified by chromatography on silica gel, eluting with hexane/ethyl acetate (5:2). Removal of solvent under vacuum gave the product 4-(1,3-dioxolan-2-yl)-butanenitrile (11.28 g; 76%) as a colorless oil. 1H NMR (CDCl3) δ 4.89-4.91 (1H, m), 3.92-4.01 (2H, m), 3.82-3.90 (2H, m), 2.40-2.46 (2H, m), 1.77-1.85 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933304B2
Source datasetuspto-grants-2005_08
ORD IDord-d97d9810ff9c4dbda1505019c5a214f6
Source noteuspto-grants-2005_08