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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960028Generated: October 29, 2026

p-Toluenesulfonic acid → (4,4-Diethoxycyclohexylmethoxymethyl)benzene

https://huagongshe.com/reaction/1960028

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTriethylamineHCID 8471—
ReactantEthyl orthoformateHCID 31214—
ReactantCyclohexanone, 4-[(phenylmethoxy)methyl]-HCID 10443381—
SolventEthanolHCID 702—
Product(4,4-Diethoxycyclohexylmethoxymethyl)benzeneHCID 57617622—

Reaction Steps

4-Benzyloxymethylcyclohexanone (168 g, 0.77 mol) is dissolved in ethanol (2000 mL), and then triethylorthoformate (350 mL) and p-toluenesulfonic acid (13.3 g) are added. The resulting mixture is stirred and refluxed for 6 hours. After addition of triethylamine (10.5 mL) at room temperature, the mixture is concentrated (500 mL). After addition of sat. NaHCO3 aq., the resulting mixture is extracted with EtOAc. The water layer is extracted with EtOAc and the combined organic layer is washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The crude mixture is purified by short pad silica gel column chromatography to afford (4,4-diethoxycyclohexylmethoxymethyl)benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410275B2
Source datasetuspto-grants-2013_04
ORD IDord-289efcd4649d4d9597efd4258cad4e7e
Source noteuspto-grants-2013_04