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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804764Generated: October 31, 2026

Potassium tert-butoxide → (2-Cyclohexa-1,3-dienyl-ethoxymethyl)-benzene

https://huagongshe.com/reaction/1804764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant[2-(1-Benzenesulfonyl-cyclohex-2-enyl)-ethoxymethyl]-benzeneHCID 59152663—
Solventtert-ButanolHCID 6386—
Product(2-Cyclohexa-1,3-dienyl-ethoxymethyl)-benzeneHCID 59152681—

Reaction Conditions

Temperature80 °C

Reaction Steps

[2-(1-Benzenesulfonyl-cyclohex-2-enyl)-ethoxymethyl]-benzene (8) (16 g, 44.9 mmol) is dissolved in tert. butanol (450 ml) and after addition of potassium tert.-butoxide (11.1 g, 98.7 mmol) the mixture is stirred for 32 h at 80° C. Then the mixture is poured on ice and extracted with pentane. The organic layer is separated, washed with saturated NaCl-solution and dried over Na2SO4. The crude product is purified by Flash-chromatography (ethyl acetate/hexanes (1:9), silicagel).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354431B2
Source datasetuspto-grants-2013_01
ORD IDord-e032fb1822074790b8b54fad0eb40f5d
Source noteuspto-grants-2013_01