HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2394325Erstellt: 24. Oktober 2026
Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamide
https://huagongshe.com/de/reaction/2394325
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Phenyl Chlorodithioformate | HCID 592675 | — |
| Edukt | N1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide | HCID 22866848 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxycarbonyl-L-valinamide | HCID 53713420 | 66% |
Reaktionsschritte
0.5 g of N-methylmorpholine was added to a suspension containing 1.4 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.9 g of phenyl chlorodithioformate was added to the mixture at -15° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and subsequently the whole mixture was stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus yielding 1.4 g of the desired product in the form of a yellow glutinous substance (yield: 66%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05811424 |
|---|
| Quelldatensatz | uspto-grants-1998_09 |
|---|
| ORD ID | ord-b83c5895d90b4eeeb48f095caf1ac85b |
|---|
| Quellennotiz | uspto-grants-1998_09 |
|---|