HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35249Erstellt: 23. Oktober 2026
Diethylamine → N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide
https://huagongshe.com/de/reaction/35249
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethylamine | HCID 8021 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | HCID 178482013 | HCID 178482013 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide | HCID 21153948 | 54% |
Reaktionsschritte
4-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (2 g) is dissolved in dry tetrahydrofuran (30 ml), and thereto is added triethylamine (1.1 g). To the mixture is added dropwise with stirring isobutyl chloroformate (1.5 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes. To the mixture is further added dropwise with stirring diethylamine (0.9 g) at room temperature, and the mixture is stirred for 2 hours. The mixture is concentrated under reduced pressure, and the resulting residue is purified by subjecting it to column chromatography (Kieselgel 60, made by Merck & Co.). By eluting with n-hexaneethyl acetate (1:1), there is obtained N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (1.4 g), colorless liquid, nD17.5 =1.5227.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04766120 |
|---|
| Quelldatensatz | uspto-grants-1988_08 |
|---|
| ORD ID | ord-78fb2885d3ea475e8b0b26aab8d14d29 |
|---|
| Quellennotiz | uspto-grants-1988_08 |
|---|