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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790010Generated: October 26, 2026

4-Hydroxybenzaldehyde → 4-Piperidin-1-ylmethyl-phenol

https://huagongshe.com/reaction/1790010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPiperidineHCID 8082—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product4-Piperidin-1-ylmethyl-phenolHCID 11636972—

Reaction Steps

A solution of 4-hydroxybenzaldehyde (10 g), piperidine (8.9 mL), and acetic acid (4.7 mL) in DCE (200 mL) was treated with sodium triacetoxyborohydride (24 g). After 16 h, the resulting mixture was treated with saturated aqueous sodium bicarbonate (100 mL) and extracted with DCM (5×100 mL). The combined organic phases were dried (magnesium sulfate) and evaporated. Trituration of the residue with ethyl acetate gave the title compound as a white crystalline solid (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071191B2
Source datasetuspto-grants-2006_07
ORD IDord-bb490914043a4089a4b4985a7be43596
Source noteuspto-grants-2006_07