HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1107099Erstellt: 26. Oktober 2026
Ethyl isovalerate → (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane
https://huagongshe.com/reaction/1107099
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl isovalerate | HCID 7945 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Lösungsmittel | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Produkt | (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane | HCID 53927273 | — |
Reaktionsschritte
Tetrahydrofuran (100 ml) and 1,3-dimethyl-3,4,5,6-tetrahydro 2 (1H)-pyrimidinone (140 ml) were mixed at -20° C. and lithium bis (trimethylsilyl) amide (1M in tetrahydrofuran, 100 ml) was added. The mixture was cooled to -70° C., ethyl isovalerate (18.75 ml) added and stirred for 1/2 hour at -70° C. Triisopropylsilyl trifluoromethane sulfonate was added and the mixture left to stir at -75° C. for 1/2 hour before warming to room temperature and stirring for 3 hours. The reaction mixture was quenched with aqueous sodium bicarbonate (8%, 150 ml) and extracted with hexane (1000 ml). The hexane extract was washed with water (4×500 ml), dried (MgSO4), filtered and concentrated in vacuo to afford a crude yellow oil containing the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06057457 |
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| Quelldatensatz | uspto-grants-2000_05 |
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| ORD ID | ord-726b5dc3d5e546078e9063c640fb4a48 |
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| Quellennotiz | uspto-grants-2000_05 |
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