HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2659Erstellt: 25. Oktober 2026
Water → 4-n-Propyl-4-phenyl-4-silacyclohexane carbaldehyde
https://huagongshe.com/reaction/2659
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Edukt | 4-Propyl-4-phenyl-4-silacyclohexanone | HCID 11831317 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-n-Propyl-4-phenyl-4-silacyclohexane carbaldehyde | HCID 21470321 | — |
Reaktionsschritte
12 g of potassium t-butoxide was added to a mixture of 35 g of methoxymethyltriphenylphosphonium chloride and 200 ml of THF to prepare an orange ylide solution. A solution of 23 g of 4-n-propyl-4-phenyl-4-silacyclohexanone in 50 ml of THF was added to the ylide solution and agitated at room temperature for 2 hours. Thereafter, the mixture was poured into iced water and extracted with methylene chloride, followed by washing, drying and concentration by a usual manner. n-Hexane was added to the residue, and the resultant crystals of triphenylphosphine oxide were removed by filtration. The filtrate was concentrated, and the resultant residue was hydrolyzed with 100 ml of 20% hydrochloric acid, followed by washing, drying and concentration by a usual manner to obtain 4-n-propyl-4-phenyl-4-silacyclohexane carbaldehyde.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05730901 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-7af0ec22991e44728c4339cf7a4c117a |
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| Quellennotiz | uspto-grants-1998_03 |
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