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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-DimethylaminopyridineHCID 21885—
Edukt2-Chloropyridin-4-amineHCID 84432—
EduktTert-butyldicarbonateHCID 22064466—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl N-(2-chloropyridin-4-yl)carbamateHCID 2185844780%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129416B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-7ff335cb7e2243f9a969bfa6844ecf0c
Quellennotizuspto-grants-2012_03