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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919561Generated: October 31, 2026

Acetic Acid → tert-Butyl(1-benzylpiperidin-3-yl)carbamate, (R)-

https://huagongshe.com/reaction/919561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantPotassium CarbonateHCID 11430—
Reactant(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Producttert-Butyl(1-benzylpiperidin-3-yl)carbamate, (R)-HCID 25417446104%

Reaction Steps

To a solution of (R)-tert-butyl piperidin-3-ylcarbamate (500 mg, 2.4 mmol) in MeOH (15 mL), AcOH (0.75 mL, 12.4 mmol) and NaCNBH3 (310 mg, 4.8 mmol) were added sequentially. To this stirred solution was added benzaldehyde (0.25 mL, 2.4 mmol) drop-wise. The reaction mixture was stirred at rt for 60 h before saturated K2CO3(aq) solution was added to neutralize it. The reaction mixture was concentrated in vacuo to give a residue which was dissolved in water and extracted with EtOAc (30 mL×3). The combined EtOAc layer was dried over Na2SO4 and concentrated in vacuo to afford the titled intermediate (725 mg, 48%) that was used in the next step without further purification. LC-MS: m/z [M+1]=291.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273028B2
Source datasetuspto-grants-2016_03
ORD IDord-aa58ee8b1d06457b93040ae73522b324
Source noteuspto-grants-2016_03