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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079004Generated: October 31, 2026

tert-Butanol → HCID 12952598, compound

https://huagongshe.com/reaction/1079004

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-HCID 11083—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMonosodium phosphateHCID 23672064—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
ProductHCID 12952598HCID 1295259840%

Reaction Steps

Ether (125 ml), t-butanol (13.2 ml) and methyltriphenylphosphonium bromide (50 g) were mixed with stirring at room temperature, then potassium t-butoxide (25.7 g) was added portionwise 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 (RS)-3-methyl-2-(2-propenyl)-4-hydroxy-cyclopent-2-ene-1-one (26.0 g) in ether (25 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 the product was 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 to afford (RS)-2-methyl-4-methylidene3-(2-propenyl)cyclopent-2-ene-1-ol (10.0 g) in a yield of 40%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550260
Source datasetuspto-grants-1996_08
ORD IDord-5c3ae12f60b74052abb2208dfb715c3d
Source noteuspto-grants-1996_08