HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49664Erstellt: 23. Oktober 2026
Tert-Butyl nitrite → 3-(2-Methyl-6-methylthiophenyl)-4,5-dihydroisoxazole
https://huagongshe.com/de/reaction/49664
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tert-Butyl nitrite | HCID 10906 | — |
| Edukt | Dimethyl Disulfide | HCID 12232 | — |
| Edukt | 2-(4,5-Dihydroisoxazol-3-yl)-3-methylaniline | HCID 9794006 | — |
| Katalysator | Copper | HCID 23978 | — |
| Produkt | 3-(2-Methyl-6-methylthiophenyl)-4,5-dihydroisoxazole | HCID 10878342 | — |
Reaktionsschritte
19.5 g (170 mmol) of tert-butylnitrite and 20 g of copper powder are initially charged in 30 ml of dimethyl disulfide, and a solution of 20 g (114 mmol) of 2-(4,5-dihydroisoxazol-3-yl)-3-methylaniline in 100 ml of dimethyl disulfide is added dropwise at from 50 to 55° C. The mixture is subsequently stirred at 60° C. for 1.5 hours. For work-up, the solid is filtered off with suction, and the filtrate is diluted with methylene chloride and extracted with dilute hydrochloric acid. The organic phase is washed with saturated aqueous NaHCO3 solution and dried over sodium sulfate, the drying agent is filtered off and the filtrate is concentrated. Excess dimethyl disulfide is removed under oil pump vacuum.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06706886B2 |
|---|
| Quelldatensatz | uspto-grants-2004_03 |
|---|
| ORD ID | ord-225b4e59ac194d10aa7e481d914525c0 |
|---|
| Quellennotiz | uspto-grants-2004_03 |
|---|