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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426535Generated: October 31, 2026

Acetic Acid → [1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2426535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventEthanolHCID 702—
Product[1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 6714736153%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of piperidin-4-yl-carbamic acid tert-butyl ester (10.0 g, 50.0 mmol, 1.0 equiv), 3-ethoxy-4-methoxy-benzaldehyde (10.8 g, 60.0 mmol, 1.2 equiv; commercially available) and acetic acid (11.4 mL, 12.01 g, 200.0 mmol, 4.0 equiv) in ethanol (40 mL) was heated by microwave irradiation to 100° C. for 5 min. Sodium cyanoborohydride (6.27 g, 100.0 mmol, 2.0 equiv), dissolved in ethanol (20 mL), was added and the reaction mixture heated by microwave irradiation to 100° C. for an additional time period of 5 min. The solvent was removed under reduced pressure and the crude reaction product extracted from a solution of 1 M NaOH (200 mL) with ethyl acetate (3×100 mL). The combined organic phases were dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with ethyl acetate to yield 9.71 g (53%) of the title compound as a white solid. MS (ISP): 365.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968568B2
Source datasetuspto-grants-2011_06
ORD IDord-8793c353e60e46efb77178a8a0807fd0
Source noteuspto-grants-2011_06