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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787702Generated: October 30, 2026

Aluminium lithium hydride → 2-Amino-1-(1-benzylpiperidin-4-yl)ethan-1-ol

https://huagongshe.com/reaction/1787702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHydroxy[1-(phenylmethyl)-4-piperidinyl]acetonitrileHCID 57599582—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-1-(1-benzylpiperidin-4-yl)ethan-1-olHCID 57599575—

Reaction Steps

To a solution of LiAlH4 (1.1 g, 28.7 mmol) in THF (25 mL) at 0° C. was added dropwise via addition funnel a solution of hydroxy[1-(phenylmethyl)-4-piperidinyl]acetonitrile (2.2 g, 9.56 mmol) in THF (25 mL). After 12 h at 25° C., the solution was carefully quenched by dropwise additional of sodium potassium tartrate and extracted several times with DCM. The combined organic fractions were dried (Na2SO4) and concentrated yielding the title compound as a yellow oil which was used without further purification: LCMS (ES) m/e 235 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511035B2
Source datasetuspto-grants-2009_03
ORD IDord-a1a82202107b4eb58f667246f28292f6
Source noteuspto-grants-2009_03