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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325059Generated: October 29, 2026

Sodium hydride → 4,4'-[Oxybis(methylene)]dibenzonitrile

https://huagongshe.com/reaction/325059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
Reactantp-Cyanobenzyl alcoholHCID 160549—
SolventTetrahydrofuranHCID 8028—
Product4,4'-[Oxybis(methylene)]dibenzonitrileHCID 13117974—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.), stirred solution of 4-cyanobenzyl alcohol (637 mg, 4.8 mmol) in dry THF (15 mL) was added a dispersion of sodium hydride in mineral oil (60%; 192 mg, 4.8 mmol), portionwise over five minutes under an argon atmosphere. The resulting milky white solution was allowed to warm to room temperature and stirred for three hours (bubbling was observed). To the resulting light green mixture was added dry dimethylformamide (3 mL) to improve homogeneity. After stirring for an additional hour, the 4-cyanobenzyl bromide (930 mg, 4.8 mmol) was added. The resulting yellow, cloudy mixture was stirred at room temperature overnight. The reaction was then carefully quenched with the addition of 1 N aqueous HCl (15 mL) and extracted with ether (3×30 mL). The combined ethereal extracts were washed with water and brine then dried (MgSO4), filtered and concentrated in vacuo to provide the desired ether as a light yellow solid (1.06 g, 89%). No further purification was necessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221914B1
Source datasetuspto-grants-2001_04
ORD IDord-4a0933a206404fe0af991886f6afa34c
Source noteuspto-grants-2001_04