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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586748Generated: October 30, 2026

Methanol → Benzyl methyl ether

https://huagongshe.com/reaction/586748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
SolventBenzeneHCID 241—
ProductBenzyl methyl etherHCID 1086993%

Reaction Steps

To a solution of 1.57 g (10 mmol) of benzyl chloride in 40 ml of benzene, 5.57 g (15 mmol) of the tris(dimethylamino)[tris(dimethylamino)phosphoranilideneamino]phosphonium salt of methanol, said salt having had been synthesized in a similar manner as in Example 1, were added at 0° C., followed by a reaction at room temperature for 3 hours. Water (50 ml) was then added to the reaction mixture to terminate the reaction. An organic layer was separated, washed successively with 20 ml of water and 20 ml of a saturated aqueous solution of sodium chloride, and then concentrated to dryness. The resulting liquid compound was distilled, whereby benzyl methyl ether, the target compound, was obtained as a colorless liquid compound in an amount of 1.13 g. Its yield was 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936684B2
Source datasetuspto-grants-2005_08
ORD IDord-997bf4f7a2b34947b56a3a5f317e00e2
Source noteuspto-grants-2005_08