HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2653Erstellt: 24. Oktober 2026
Water → 4-n-Heptyl-4-phenyl-4-silacyclohexane carbaldehyde
https://huagongshe.com/de/reaction/2653
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Edukt | 4-n-Heptyl-4-phenyl-4-silacyclohexanone | HCID 19593797 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-n-Heptyl-4-phenyl-4-silacyclohexane carbaldehyde | HCID 53830843 | — |
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 28 g of 4-n-heptyl-4-phenyl-4-silacyclohexanone in 50 ml of THF was added to the solution. After agitation for 2 hours at room temperature, the mixture was poured into iced water and extracted with methylene chloride. The extract was washed, dried and concentrated by a usual manner. n-Hexane was added to the resultant concentrate, followed by removal of the resultant triphenylphosphine oxide crystals by filtration. The resultant filtrate was concentrated. The concentrate was hydrolyzed with 100 ml of 20% hydrochloric acid, followed by washing, drying and concentration by a usual manner to obtain 4-n-heptyl-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-185154b6627f4f909d32b9149fae48a3 |
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| Quellennotiz | uspto-grants-1998_03 |
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