HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2369715Erstellt: 24. Oktober 2026
Cyclopentanethiol → Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilane
https://huagongshe.com/de/reaction/2369715
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyclopentanethiol | HCID 15510 | — |
| Edukt | Tert-butyl[(3-iodobenzyl)oxy]dimethylsilane | HCID 66845200 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | Tert-butyl([3-(cyclopentylthio)benzyl]oxy}dimethylsilane | HCID 66845801 | 82,2% |
Reaktionsschritte
Tert-butyl[(3-iodobenzyl)oxy]dimethylsilane (WO9513095) (1.44 g) in dry 1-methyl-2-pyrrolidone (15 ml) and triethylamine (4 ml) was stirred at room temperature under nitrogen. 1-1′Bis(diphenylphosphino)ferrocene (110 mg) and tris(dibenzylideneacetone)dipalladium(0) (258 mg) were added and the mixture was stirred for 15 min. Cyclopentyl mercaptan (0.42 g) was then added, and the reaction mixture stirred at 60° C. for 2 h. The reaction mixture was cooled to room temperature, poured onto water and extracted with diethyl ether. The combined organic extracts were dried (MgSO4) and the solvent evaporated in vacuo. The residue was purified on a 50 g SPE, eluting with a stepped gradient of 10 to 100% dichloromethane-cyclohexane to give the title compound (1.09 g) LCMS RT=4.67 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | USRE044874E1 |
|---|
| Quelldatensatz | uspto-grants-2014_04 |
|---|
| ORD ID | ord-d75dd3502e0e460c9fe2eefae1782a8c |
|---|
| Quellennotiz | uspto-grants-2014_04 |
|---|