HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5621Erstellt: 23. Oktober 2026
Trifluoromethanesulfonic acid → Methyl (3R)-3-(benzyloxy)tetradecanoate
https://huagongshe.com/de/reaction/5621
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Edukt | Benzyl 2,2,2-trichloroacetimidate | HCID 144968 | — |
| Edukt | 3R-hydroxymyristic acid methyl ester | HCID 9834945 | — |
| Lösungsmittel | Cyclohexane | HCID 8078 | — |
| Produkt | Methyl (3R)-3-(benzyloxy)tetradecanoate | HCID 13817922 | 112,8% |
Reaktionsschritte
A suspension of 206.7 g of methyl (R)-3-hydroxytetradecanoate in 1000 ml of cyclohexane was treated under nitrogen and while stirring with 214.2 g of benzyl trichloroacetimidate and dissolved at 20°. 10 ml of trifluoromethanesulphonic acid were added dropwise while cooling in an ice/water bath in such a manner that the temperature remains between 20°-23°. The resulting suspension was stirred at 25°-30°. The precipitate was filtered off, the filter cake was washed with cyclohexane, the filtrates were extracted with sat. NaHCO3 solution, water and sat. NaCl solution. The organic phase was dried over magnesium sulphate, filtered, the filter cake was washed with cyclohexane and the filtrates were evaporated. 314.5 g of methyl (R)-3-(benzyloxy)-tetradecanoate were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05245056 |
|---|
| Quelldatensatz | uspto-grants-1993_09 |
|---|
| ORD ID | ord-7aa6ea05ad5f4e639b91d1a44ecf298b |
|---|
| Quellennotiz | uspto-grants-1993_09 |
|---|