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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404398Generated: November 1, 2026

Benzyl Bromide → 8-[2-(Benzyloxy)ethyl]-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/1404398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-(1,4-Dioxaspiro(4.5)decan-8-yl)ethan-1-olHCID 11805458—
SolventTetrahydrofuranHCID 8028—
Product8-[2-(Benzyloxy)ethyl]-1,4-dioxaspiro[4.5]decaneHCID 2187960383.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a precooled (0° C.) suspension of NaH (60% in mineral, 0.44 g, 11 mmol) in THF (20 mL) was added 2-(1,4-dioxaspiro[4.5]decan-8-yl)ethanol (1.86 g, 10 mmol) in THF (10 mL). The resulting solution was stirred at 0° C. for 10 min, and allowed to warm to RT, and stirred for 1 h. To the above mixture was added benzyl bromide (1.78 g, 15 mmol) and the resulting mixture was stirred at rt overnight. The reaction was quenched by addition of saturated aqueous NH4Cl solution, extracted with EtOAc, washed with brine, dried over Na2SO4. Purification by flash column chromatography (eluent: 20% EtOAc in hexanes to 30%) gave the product (2.3 g, 83%). LC/MC: 277.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912169B2
Source datasetuspto-grants-2014_12
ORD IDord-3411e54154b74f65b7983bd2fe61d6a9
Source noteuspto-grants-2014_12