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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758165Generated: November 2, 2026

Ethanol → 3-Ethoxycyclohept-2-en-1-one

https://huagongshe.com/reaction/1758165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantCycloheptane-1,3-dioneHCID 4072367—
SolventTolueneHCID 1140—
Product3-Ethoxycyclohept-2-en-1-oneHCID 1567065193%

Reaction Steps

A solution of 22.3 g. (0.177 mole) of cycloheptan-1,3-dione and 600 mg. (3.16 mmoles) of p-toluenesulfonic acid monohydrate in 86 ml. of ethanol and 250 ml. of toluene was heated at reflux for B 18 hours. A soxhlet extractor filled with molecular sieves (3 A) was used to remove water from the reaction. The reaction was cooled, added to 800 ml. saturated sodium chloride and extracted with four 800 ml. portions of ether. The combined organic extract was dried over magnesium sulfate and evaporated to an oil. Distillation of the crude oil gave 25.3 g. (93%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371720
Source datasetuspto-grants-1983_02
ORD IDord-5366c46425844680be2b1aa4024a8c97
Source noteuspto-grants-1983_02