HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 400630Erstellt: 26. Oktober 2026
Cesium fluoride → 2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol
https://huagongshe.com/reaction/400630
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Cesium fluoride | HCID 25953 | — |
| Edukt | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Edukt | 3-(5-Fluoro-2-methoxyphenyl)-3-methylbutyraldehyde | HCID 57809896 | — |
| Edukt | (1-Fluorovinyl)dimethylphenylsilane | HCID 60026366 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol | HCID 60026610 | 59,9% |
Reaktionsschritte
To a solution of 3-(5-fluoro-2-methoxyphenyl)-3-methylbutyraldehyde (1.1 g, 5.2 mmol) and the above (1-fluorovinyl)dimethylphenylsilane (2.2 g, 12.2 mmol) in 5 mL of THF was added 0.6 mL of tetrabutylammonium fluoride (1 M in THF) and the mixture was stirred at room temperature overnight. TLC showed partial conversion to product. Cesium fluoride (0.22 g) was added and the mixture was stirred at room temperature for 3 days. 2 mL of water and 2 mL of acetic acid were added and the mixture was warmed at 60° C. for 2 hours to effect desilylation of any silylated product. The mixture was diluted with ethyl acetate, washed with water, dried, filtered and concentrated in vacuo. Fractionation of the residue over silica gel (eluent: hexanes-dichloromethane (3:1 to 1:3 gradient) gave 0.798 g (59.5% yield) of 2-fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol as an oil which was used without additional purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08741897B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-9cdcad5474b1446cbfeac0a9d9ddc0cf |
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| Quellennotiz | uspto-grants-2014_06 |
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