HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 656208Erstellt: 24. Oktober 2026
Diisopropylethylamine → 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone
https://huagongshe.com/de/reaction/656208
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Edukt | 4-(2-Hydroxyethyl)cyclohexan-1-one | HCID 15700392 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone | HCID 21986099 | — |
Reaktionsschritte
A solution of 4-(2-hydroxy-ethyl)-cyclohexanone (Intermediate R10, 6.8 g, 52.6 mmol, (obtainable as described in the publication by Ciufolini et. al. J. Amer. Chem. Soc. 1991, 113, 8016) was dissolved in CH2Cl2 (75 mL) and treated with diisopropylethylamine (9.2 mL, 52.6 mmol) followed by tri-isopropylsilyl trifluoromethane sulfonate (TIPSTf) (15.3 g, 50.2 mmol) at −30° C. The reaction mixture was warmed to 0° C. for 1 h. The mixture was subjected to an aqueous work-up and purified by chromatography on SiO2 to give 4-(2-triisopropylsilanyloxy-ethyl)-cyclohexanone (Intermediate R11, 11.8 g (82%). Intermediate R11 was converted via Intermediate R12 to the unsaturated aldehyde, 5-(2-triisopropylsilanyloxy-ethyl)-cyclohex-1-enecarbaldehyde (Intermediate R13)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08071635B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-cbb4a56e9ade4183acb257439426d48b |
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| Quellennotiz | uspto-grants-2011_12 |
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