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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223719Generated: October 30, 2026

Benzaldehyde → HCID 17956592, compound

https://huagongshe.com/reaction/2223719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAcetone CyanohydrinHCID 6406—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-Benzyl-4-piperidinolHCID 98152—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 17956592HCID 17956592—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 4-benzyl-piperidin-4-ol (1.0 g, 5.2 mmol), benzaldehyde (0.83 g, 7.8 mmol) and MgSO4 (0.31 g, 2.6 mmol) in 1-methyl-2-pyrrolidone (5 mL) is added acetone cyanohydrine (0.45 g, 5.2 mmol). The reaction mixture is heated at 50° C. for 2 h, then cooled to room temperature and quenched with ice (20 g) and sat. NaHCO3 (50 mL). The aqueous phase is extracted with Et2O (3×100 mL), the combined organic extracts are washed with sat. NaCl (20 mL), dried (Na2SO4), filtered and evaporated. The residue is dissolved in THF (20 mL) and added to a suspension of LiAlH4 (1.1 g, 27.6 mmol) in THF (80 mL) at 0° C. The reaction mixture is stirred for 15 h at room temperature and quenched with EtOAc (250 mL), MeOH (20 mL) and sat. NaHCO3 (5 mL). The precipitate is filtered off, washed with MeOH (20 mL) and the filtrate evaporated. Purification by preparative HPLC provides the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375227B2
Source datasetuspto-grants-2008_05
ORD IDord-318cc3a9954542c4bd222663c520cbbb
Source noteuspto-grants-2008_05