HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 65434Erstellt: 24. Oktober 2026
Tetrabutylammonium Fluoride Trihydrate → HCID 18604777, Verbindung
https://huagongshe.com/de/reaction/65434
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Edukt | N-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amide | HCID 56993841 | — |
| Edukt | ammonium fluoride THF | HCID 69831023 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 18604777 | HCID 18604777 | — |
Reaktionsschritte
A solution of 197 mg (0.757 mmol) of N-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amide in 1 ml of tetrahydrofuran is introduced at 0°, with the exclusion of moisture, into 8 ml of a tetra-n-butyl; ammonium fluoride/THF solution which has been prepared from 5.0 g of tetra-n-butylammonium fluoride trihydrate by dehydrating at 60° C./0.1 torr and making up to 20 ml with tetrahydrofuran. The reaction mixture is stirred for 2 hours at room temperature and then partitioned between methylene chloride and phosphate buffer solution (pH 8.0). The crude product obtained by drying over sodium sulphate and concentration by evaporation of the organic phase is chromatographed over preparative silica gel plates using hexane/ethyl acetate (1:3). the title compound is obtained in the form of colourless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04614614 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-4aba25dbbd1344a8bc8c659123e7942c |
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| Quellennotiz | uspto-grants-1986_09 |
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