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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871475Generated: October 30, 2026

Ethylene Glycol → 2-(2-Isopropyl-1,3-dioxolan-2-yl)acetonitrile

https://huagongshe.com/reaction/871475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methyl-3-oxopentanenitrileHCID 10129921—
SolventDichloromethaneHCID 6344—
Product2-(2-Isopropyl-1,3-dioxolan-2-yl)acetonitrileHCID 6687672178%

Reaction Conditions

Temperature40 °C

Reaction Steps

4-Methyl-3-oxopentanenitrile was added to a mixture of ethylene glycol (4.7 mL, 84 mmol) and chlorotrimethylsilane (10.6 mL, 84 mmol) in anhydrous dichloromethane (50 mL). The mixture was stirred at 40° C. overnight. After cooling to room temperature a solution of 5% sodium bicarbonate (50 mL) was added, the layer were separated and the water phase back extracted three times with diethyl ether. The organics were combined, dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane/ethyl acetate 8:2) to afford 2-(2-isopropyl-1,3-dioxolan-2-yl)acetonitrile (3.38 g, 78%) as a colorless oil. 1H NMR (300 MHz, CDCl3) δ 4.21-4.16 (m, 2H), 4.07-3.99 (m, 2H), 2.69 (s, 2H), 2.08-2.01 (m, 1H), 0.96 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-a8bbbd52590c42eab36dcfe8d298fb5f
Source noteuspto-grants-2015_03