HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49344Erstellt: 24. Oktober 2026
Triethylamine → [(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilane
https://huagongshe.com/de/reaction/49344
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Dimethylaminopyridine | HCID 21885 | — |
| Edukt | Triethylsilyl trifluoromethanesulphonate | HCID 2733308 | — |
| Edukt | (e)-7-(4-Bromo-2-thienyl)-3-ethylnon-6-en-3-ol | HCID 69824523 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | [(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilane | HCID 69825241 | — |
Reaktionsschritte
11.8 g (35.6 mmol) of (E)-7-(4-bromo-2-thienyl)-3-ethylnon-6-en-3-ol are dissolved in 150 mL of dichloromethane. 130 mg (1.1 mmol) of dimethylaminopyridine and 14.9 mL (107 mmol) of triethylamine are added. The reaction medium is cooled to 0° C. and 12.1 mL (53.4 mmol) of triethylsilyl trifluoromethanesulphonate are added dropwise. The medium is warmed to room temperature and stirred for 15 minutes, after which it is poured into 150 mL of water and extracted with dichloromethane. After chromatography on silica gel (eluent: heptane), the desired product is obtained in the form of a colourless oil (m=15 g; Y=100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06706725B1 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-61c3221b133044d69ab1c621e42a83c4 |
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| Quellennotiz | uspto-grants-2004_03 |
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