HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1588714Erstellt: 26. Oktober 2026
Tetrabutylammonium Fluoride → alpha-Ethynylbenzenemethanol
https://huagongshe.com/reaction/1588714
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Edukt | 1-Phenyl-3-(trimethylsilyl)-2-propyn-1-ol | HCID 2760416 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | alpha-Ethynylbenzenemethanol | HCID 20155 | 81,3% |
Reaktionsschritte
Place a mixture of α-[(trimethylsilyl)ethynyl]-benzene-methanol (4.09 g, 20 mmol) and tetrahydrofuran (25 mL) under argon atmosphere and cool to 0° C. Add, by dropwise addition, tetra-n-butylammonium fluoride (25 mL of a 1M solution in tetrahydrofuran, 25 mmol). Allow to warm to room temperature and stir for 1 hour. Partition between ethyl ether and water. Separate the organic phase, wash with saturated aqueous sodium chloride and concentrate in vacuo. Purify by silica gel chromatography (15% ethyl acetate/hexane) then purify further by distillation to yield 2.15 g of the title compound; bp 100°-110° C. @0.1 mm Hg.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05223518 |
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| Quelldatensatz | uspto-grants-1993_06 |
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| ORD ID | ord-3a223550e8214c68a932503169f4d82d |
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| Quellennotiz | uspto-grants-1993_06 |
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