HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275550Erstellt: 25. Oktober 2026
Trimethylsilylacetylene → Diethyl trimethylsilylethynylphosphonite
https://huagongshe.com/reaction/275550
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | Ethyl phosphorochloridite | HCID 68530 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Diethyl trimethylsilylethynylphosphonite | HCID 53804595 | — |
Reaktionsschritte
n-Butyllithium (26.02 ml, 1.55M in hexane) was added dropwise over thirty minutes to a stirred solution of trimethylsilylacetylene (5.18 ml) in dry tetrahydrofuran (25 ml), whilst maintaining the temperature below -65° C. After twenty minutes, diethylchlorophosphite (4.71 ml) was added dropwise over twenty minutes, then stirring continued for a further ninety minutes at -65° C. The stirred mixture was allowed to warm to -20° C., quenched by dropwise addition of saturated ammonium chloride solution (10 ml), then allowed to reach room temperature, diluted with water (10 ml) and extracted with chloroform (4×25 ml). The extracts were dried over magnesium sulphate and evaporated under reduced pressure to give diethyl trimethylsilylethynylphosphonite as a brown oil (7.34 g, 83% pure by GC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05393732 |
|---|
| Quelldatensatz | uspto-grants-1995_02 |
|---|
| ORD ID | ord-01b0f93d550c45e19bf61efdb1888782 |
|---|
| Quellennotiz | uspto-grants-1995_02 |
|---|