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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376912Generated: October 25, 2026

Diethyl Ether → 2-((1-Naphthalenyloxy)methyl)oxirane

https://huagongshe.com/reaction/376912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-NaphtholHCID 7005—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-((1-Naphthalenyloxy)methyl)oxiraneHCID 91521—

Reaction Steps

A stirred suspension of sodium hydride (4.0 g of 60% NaH in mineral oil, 100 mmol) in dimethylformamide (DMF, 100 ml) was treated with 1-naphthol (14.42 g, 100 mmol). After stirring for 1 hour at ambient temperature (room temperature), the reaction was treated with epichlorohydrin (10.18 g, 110 mmol) and stirred for 1 hour at 100° C. The reaction was diluted with water and transferred to a separatory funnel using diethyl ether (500 ml). The organic phase was washed with 10% aqueous NaHCO3 (3×200 ml), dried over anhydrous sodium sulfate, filtered, and concentrated. Kugelrohr distillation (~100 microns) yielded 1-naphthyl glycidyl ether as a clear, colorless oil: GC/EI-MS, m/z (rel. int.) 200 (M+, 61), 184 (1), 169 (5), 157 (12), 144 (79), 129 (16), 115 (100), 101 (3), 89 (16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022894
Source datasetuspto-grants-2000_02
ORD IDord-3ff35f1e5b2845aca56fea04ded66e1d
Source noteuspto-grants-2000_02