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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654487Generated: October 25, 2026

p-Toluenesulfonic acid → 2-(2-Benzyloxyethoxy)-cyclohexanone

https://huagongshe.com/reaction/1654487

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantCyclohexanone, 2-hydroxy-HCID 10785—
ReactantBenzyloxyethanolHCID 19595026—
SolventO-XyleneHCID 7237—
Product2-(2-Benzyloxyethoxy)-cyclohexanoneHCID 2007796067.1%

Reaction Steps

A mixture of dimeric 2-hydroxycyclohexanone (13.7 g), 2 benzyloxyethanol (20 g) and p-toluensulphonic acid (2 g) were dissolved in xylene (500 ml) in a round bottom flask fitted with a Dean Stark apparatus and reluxed for 10 hrs. The resulting solution was cooled, washed with sodium hydrogen carbonate (3×50 ml) dried and concentrated under reduced pressure. The crude oil was then purified by flash chromatography using cyclohexane/ethyl acetate 60/40 as eluant yielding 20 g of the title compound (Rf=0.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407931
Source datasetuspto-grants-1995_04
ORD IDord-465f23e0acd14dcb8bd9ce9fcb10622f
Source noteuspto-grants-1995_04