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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 3-Isobutoxy-5-(3-(2-((triisopropylsilyl)oxy)ethyl)benzyl)cyclopent-2-enone | HCID 54757658 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-(2-Hydroxyethyl)benzyl)-3-isobutoxycyclopent-2-enone | HCID 54757659 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530520B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-7d2bf8746c5b4c22b06a6bed937bb015 |
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| Source note | uspto-grants-2013_09 |
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