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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 517669Erstellt: 25. Oktober 2026

Sulfuric Acid → (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine

https://huagongshe.com/reaction/517669

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPotassium BicarbonateHCID 516893—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt(2S)-5-[(benzyloxy)imino]-2-cyanopiperidineHCID 90088575—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(2S)-5-[(benzyloxy)amino]-2-cyanopiperidineHCID 11759934588%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Sulphuric acid (11.7 ml, 0.217 mol) was slowly added to a stirred solution of (2S)-5-[(benzyloxy)imino]-2-cyanopiperidine (IX) (10 gm, 0.0436 mol, prepared according to the procedure described in step 6) in ethyl acetate (150 ml) at −10° C. After 10 minutes of stirring, sodium triacetoxy borohydride (NaHB(OOCCH3)3) (11.7 gm, 0.0519 mol, 95% purity) was added in small portions while maintaining temperature below −5° C. After completion of the addition, stirring was further continued for 2 hour at the same temperature. The pH of the reaction mixture was adjusted to about pH 7 by using 30% aqueous potassium hydrogen carbonate solution. The mixture was allowed to warm to 25° C. and the reaction mixture was filtered under suction. The organic layer was separated and the aqueous layer extracted with fresh ethyl acetate (50 ml). The combined organic layer was washed with water (50 ml) and brine (50 ml), dried over anhydrous sodium sulphate and the solvent evaporated under reduced pressure to obtain 8.88 gm of (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (X) as an oil, in 88% yield. This was used as such for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115131B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-11cd144b00c34a06b286f049aa7d3018
Quellennotizuspto-grants-2015_08