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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 733092Erstellt: 25. Oktober 2026

Acetic Acid → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylate

https://huagongshe.com/reaction/733092

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium BicarbonateHCID 516892—
EduktTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktMethyl 1-formylcyclobutane-1-carboxylateHCID 15656335—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylateHCID 6723339183,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a stirred mixture of tert-butyl(piperidin-4-ylmethyl)carbamate (12.8 g, 60 mmol) and methyl 1-formylcyclobutanecarboxylate (2.13 g, 15 mmol, Davis, Charles R.; Swenson, Dale C.; Burton, Donald J., J. Org. Chem., 1993, 58, 6843) in tetrahydrofuran (50 mL) was added acetic acid (8.6 mL, 150 mmol) at ambient temperature. After 30 min, sodium triacetoxyborohydride (12.7 g, 60 mmol) was added to the mixture. Then, the mixture was heated to 60° C. for 2 h. After cooling, the reaction mixture was poured into sat. NaHCO3 aq. The aqueous layer was extracted with CH2Cl2 for 3 times. The combined organic phase were washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 4.25 g (83%) of the title compound as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07589109B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-7d351ffb7d2645e6b188a7254df7a931
Quellennotizuspto-grants-2009_09