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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527013Generated: October 26, 2026

Water → ((Cyclohex-2-enyloxy)methyl)benzene

https://huagongshe.com/reaction/527013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
Reactant2-Cyclohexen-1-OLHCID 13198—
ReactantSodium hydrideHCID 24758—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product((Cyclohex-2-enyloxy)methyl)benzeneHCID 10867111—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of cyclohex-2-en-1-ol (10.0 g, 101.9 mmol) in anhydrous THF (100 mL) was added to a stirred suspension containing sodium hydride (8.0 g, 199.7 mmol) (60% dispersion in oil) and benzyl bromide in anhydrous THF (250 mL) maintained at 50° C. The resulting solution was stirred at 55-60° C. for 18 h. After cooling to ambient temperature, water was added to quench the reaction and the mixture was diluted with ether (500 mL). The organic phase was separated, dried (Na2SO4), filtered and concentrated in vacuo to an oil that was subjected to a short silica plug filtration to provide 16.1 g of desired product 51a that was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345708B2
Source datasetuspto-grants-2016_05
ORD IDord-b10b40a6bab840a290a8c20455a598f0
Source noteuspto-grants-2016_05