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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1743006Erstellt: 25. Oktober 2026

Ammonium Chloride → tert-Butyl 3-azidopiperidine-1-carboxylate

https://huagongshe.com/reaction/1743006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktSodium AzideHCID 33557—
EduktN-Boc-3-mesyloxypiperidineHCID 568122—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-Butyl 3-azidopiperidine-1-carboxylateHCID 54772256,8%

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

Sodium azide (6.96 g, 0.107 mol) and ammonium chloride (2.13 g, 0.0399 mol) were added to a solution of 1-(tert-butoxy carbonyl)3-[(methylsulphonyl)oxy]piperidine (10 g, 0.0358 mol) in DMF (75 ml) and water (12.5 ml). The mixture was heated overnight at 125° C. under stirring, cooled and diluted with water and extracted with chloroform. The organic layer was washed with water, dried over Na2SO4 and concentrated to give 4.6 g of thin reddish brown oil. 1H NMR (CDCl3) δ: 2.80-4.30 (m, 5H), 1.60-2.20 (m, 4H), 1.50 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05342846
Quelldatensatzuspto-grants-1994_08
ORD IDord-a7e833bf4c6b4922ae2e52e8ed4420da
Quellennotizuspto-grants-1994_08