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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203710Generated: November 1, 2026

Acetic Acid → Diethyl trans-1-benzyl-4-methoxypiperidin-3-ylphosphoramidate

https://huagongshe.com/reaction/2203710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67045828HCID 67045828—
SolventMethanolHCID 887—
ProductDiethyl trans-1-benzyl-4-methoxypiperidin-3-ylphosphoramidateHCID 6704528998%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of diethyl trans-4-methoxypiperidin-3-ylphosphoramidate (1.30 g, 4.88 mmol), benzaldehyde (0.74 mL, 7.32 mmol) and acetic acid (0.56 mL, 9.76 mmol) in methanol (20 mL) was stirred at 0° C. for 30 minutes. NaCNBH3 (0.46 g, 7.32 mmol) was added at 0° C. The resulting solution was warmed to room temperature and stirred at room temperature for 1 hour. The solvent was removed in vacuo and saturated sodium bicarbonate (20 mL) and ethyl acetate (30 mL) were added. The organic layer was separated, washed with brine, dried (sodium sulfate) and concentrated in vacuo to give diethyl trans-1-benzyl-4-methoxypiperidin-3-ylphosphoramidate (1.70 g, 98%), which was used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-31b86f754a214113bdda814f917f0ec3
Source noteuspto-grants-2016_06