HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 5-(S)-methyl-7-(t-butyldimethylsilyloxy)-2-heptene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanal | HCID 10443866 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Phosphonium, ethyltriphenyl-, bromide (1:1) | HCID 73727 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-(S)-methyl-7-(t-butyldimethylsilyloxy)-2-heptene | HCID 53780377 | — |
Reaktionsschritte
To a slurry of 80 g. (0.2155 m) of triphenyl-ethyl phosphonium bromide in 800 ml. of dry tetrahydrofuran cooled to 0° C. was added 165.7 ml. of 1.3M solution of n-butyl lithium (0.2155 m) in the same solvent. After 2 hours, 45 g. (0.196 m) 3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanal in 200 ml. of dry tetrahydrofuran was added dropwise to the reaction mixture. The reaction was allowed to stir 2 hours at room temperature and was then poured into water and extracted with ether. The combined extracts were washed with water and a brine solution and dried over magnesium sulfate. Removal of the solvent in vacuo gave a yellow oil which, on distillation gave 37.4 g. of product, b.p. 74°-79° C./0.2-0.1 torr.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04767743 |
| Quelldatensatz | uspto-grants-1988_08 |
| ORD ID | ord-4c5114fdff2d45a59c871c8312f0440a |
| Quellennotiz | uspto-grants-1988_08 |