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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917874Generated: October 31, 2026

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

https://huagongshe.com/reaction/1917874

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 numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-fc739c4446a04b938a18833b2666ac1f
Source noteuspto-grants-2013_12