Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733092Generated: October 25, 2026

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

https://huagongshe.com/reaction/733092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 1-formylcyclobutane-1-carboxylateHCID 15656335—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylateHCID 6723339183.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589109B2
Source datasetuspto-grants-2009_09
ORD IDord-7d351ffb7d2645e6b188a7254df7a931
Source noteuspto-grants-2009_09