Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265298Generated: October 30, 2026

2-Benzyl-1,3-dioxolane → HCID 19082234, compound

https://huagongshe.com/reaction/265298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzyl-1,3-dioxolaneHCID 7562—
ReactantSodium HydroxideHCID 14798—
Reactant3-BromopropionitrileHCID 17020—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 19082234HCID 1908223490%

Reaction Steps

A mixture of 3-(2-phenylethoxy)ethanol (8.0 g, prepared from 2-phenylmethyl 1,3-dioxolane according to the general method in Can. J. Chem., 1974, 52, 888), 3-bromopropanenitrile (5.6 ml), sodium hydroxide (50 g) and tetrabutylammonium chloride (0.5 g) in dichloromethane (100 ml) and water (100 ml) was stirred at room temperature for 72 hours. The mixture was diluted with water and the organic layer separated. The aqueous layer was extracted with a further portion of dichloromethane. The combined organic extracts were washed with dilute aqueous hydrochloric acid and water, dried (MgSO4) and evaporated under reduced pressure to yield the crude product. This material was purified by flash chromatography over silica using 1:1 ether:petroleum ether (bp 60°-80°) as eluant to give the subtitled compound as an oil (9.84 g, 90% ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648370
Source datasetuspto-grants-1997_07
ORD IDord-00d7d368ac524d61bd2219f2643035b6
Source noteuspto-grants-1997_07