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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079005Generated: October 29, 2026

tert-Butanol → (S)-2-methyl-4-methylidene-3-(2-propynyl)cyclopent-2-ene-1-ol

https://huagongshe.com/reaction/1079005

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant4-Hydroxy-3-methyl-2-(prop-2-yn-1-yl)cyclopent-2-en-1-oneHCID 156997—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMonosodium phosphateHCID 23672064—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
Product(S)-2-methyl-4-methylidene-3-(2-propynyl)cyclopent-2-ene-1-olHCID 11829602—

Reaction Steps

Ether (70 ml), t-butanol (6.6 ml) and methyltriphenylphosphonium bromide (25 g) were mixed with stirring at room temperature, then potassium t-butoxide (12.9 g) was added to the mixture and then the resulting solution was stirred for 5 hours at the same temperature. To the solution was added a solution of (S)-3-methyl-2-(2-propynyl)-4-hydroxycyclopent-2-ene-1one (12.42 g) in ether (13 ml) under ice-water cooling and the resulting reaction mixture was stirred at the same temperature for 2 hours and then for 6 hours at room temperature. The reaction solution was poured into a saturated aqueous solution of sodium dihydrogenphosphate, and extracted with ether. The obtained ether layer was washed with brine and dried over anhydrous magnesium sulfate. Then the filtered solution was evaporated. The obtained oily residue was then subjected to silica gel column chromatography, however, neither the desired product, (S)-2-methyl-4-methylidene-3-(2-propynyl)cyclopent-2-ene-1-ol nor the starting material was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550260
Source datasetuspto-grants-1996_08
ORD IDord-8aef7ceff4d545dfa23aacad2158acfb
Source noteuspto-grants-1996_08