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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203718Generated: November 1, 2026

Acetic Acid → HCID 67045005, compound

https://huagongshe.com/reaction/2203718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67045765HCID 67045765—
SolventMethanolHCID 887—
ProductHCID 67045005HCID 6704500599%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of diethyl trans-4-fluoropiperidin-3-ylphosphoramidate (0.35 g, 1.38 mmol), benzaldehyde (0.21 mL, 2.07 mmol) and acetic acid (0.16 mL, 2.75 mmol) in methanol (20 mL) was stirred at 0° C. for 30 minutes. NaCNBH3 (0.13 g, 2.07 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-fluoropiperidin-3-ylphosphoramidate (0.47 g, 99%), 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-7a62c365c7c942928950c1aa583811d0
Source noteuspto-grants-2016_06