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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603871Generated: October 30, 2026

Water → 2-(Benzyloxymethyl)chromane

https://huagongshe.com/reaction/1603871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-(Hydroxymethyl)chromanHCID 2794816—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxymethyl)chromaneHCID 1960631583%

Reaction Steps

A suspension of 60% sodium hydride dispersion in mineral oil (0.711 g, 17.8 mmol, previously washed with dry petroleum ether) in dry N,N-dimethylformamide (30 ml) was added; under inert atmosphere, with 2-chromanemethanol (1.218 g, 7.43 mmol) dissolved in N,N-dimethylformamide (15 ml) and the mixture was left under stirring at room temperature for 1 h. After that a solution of benzyl hbromide (2.12 ml, 17.8 mmol) in N,N-dimethylformamide (20 ml) and some crystals of tetrabutylammonium iodide were added stirring at room temperature for 18 h. Afterwards, water (10 ml) was added and the solvent was evaporated off under reduced pressure. The obtained residue was partitioned in a mixture of water (70 ml) and ethyl ether (70 ml), the phases were separated and the aqueous one was extracted with ethyl ether (3×70 ml). The combined organic phases were dried and the solvent was evaporated off under reduced pressure, to obtain a crude which was purified by flash chromatography through a silica gel column. Eluting with petroleum ether:ethyl ether, 9:1, 1.569 g of the title product were recovered (83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990142
Source datasetuspto-grants-1999_11
ORD IDord-978fec21fdd54f2684dee8a0826ea5c0
Source noteuspto-grants-1999_11