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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41141Generated: October 29, 2026

Tetrabutylammonium Fluoride → 5-(3-(2-Hydroxyethyl)benzyl)-3-isobutoxycyclopent-2-enone

https://huagongshe.com/reaction/41141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant3-Isobutoxy-5-(3-(2-((triisopropylsilyl)oxy)ethyl)benzyl)cyclopent-2-enoneHCID 54757658—
SolventTetrahydrofuranHCID 8028—
Product5-(3-(2-Hydroxyethyl)benzyl)-3-isobutoxycyclopent-2-enoneHCID 5475765982%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tetrabutylammonium fluoride (1 M in tetrahydrofuran, 0.47 mL, 0.47 mmol) was added dropwise to an ice-water bath cooled solution of 20 (0.071 g, 0.16 mmol) in anhydrous tetrahydrofuran (1 mL). The reaction mixture was stirred at 0° C. for 3 h and then quenched with a saturated solution of ammonium chloride. The two phases were separated and the aqueous layer was extracted with diethyl ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by silica gel column chromatography using dichloromethane-methanol 95:5 as eluent to provide the desired product as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530520B2
Source datasetuspto-grants-2013_09
ORD IDord-7d2bf8746c5b4c22b06a6bed937bb015
Source noteuspto-grants-2013_09