HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1092281Erstellt: 25. Oktober 2026
Triethylamine → tert-butyl N-(2-chloropyridin-4-yl)carbamate
https://huagongshe.com/reaction/1092281
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Dimethylaminopyridine | HCID 21885 | — |
| Edukt | 2-Chloropyridin-4-amine | HCID 84432 | — |
| Edukt | Tert-butyldicarbonate | HCID 22064466 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | tert-butyl N-(2-chloropyridin-4-yl)carbamate | HCID 21858447 | 80% |
Reaktionsschritte
1.69 g (7.78 mmol, 1 eq) of tert-butyl dicarbonate dissolved in 50 ml of dichloromethane, in the presence of 95 mg of dimethylaminopyridine, are added to a solution of 1 g (7.78 mmol, 1 eq) of 4-amino-2-chloropyridine in 30 mL of dichloromethane in the presence of 1.19 mL (1.19 mmol, 1.1 eq) of triethylamine. The reaction mixture is stirred overnight at room temperature. The reaction is stopped by adding 100 ml of water and is then extracted with dichloromethane. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 to 50/50 heptane/ethyl acetate). The oil obtained is crystallized from pentane. 1.40 g of tert-butyl (2-chloropyrid-4-yl)carbamate are obtained. Yield=80%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08129416B2 |
|---|
| Quelldatensatz | uspto-grants-2012_03 |
|---|
| ORD ID | ord-7ff335cb7e2243f9a969bfa6844ecf0c |
|---|
| Quellennotiz | uspto-grants-2012_03 |
|---|