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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093051Generated: November 4, 2026

Methanol → (1-Benzylpiperidine-3,5-diyl)dimethanol

https://huagongshe.com/reaction/1093051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantDimethyl 1-benzylpiperidine-3,5-dicarboxylateHCID 57905194—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzylpiperidine-3,5-diyl)dimethanolHCID 5790499475.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To dimethyl 1-benzylpiperidine-3,5-dicarboxylate (1.5 g, 5.15 mmol) in dry THF (30 mL) was added a solution of lithium aluminum hydride in THF (2M, 3.87 mL, 7.73 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 30 min. then warmed to 23° C. and stirred for 1.5 hour. A solution of methanol (0.5 mL) and (0.25 mL) was added followed by a 15% solution of NaOH (0.250 mL). The mixture was stirred for 1 hour at 23° C. then filtered. The organic material was extracted with ethyl acetate (3×20 mL) and the combined extracts were dried (MgSO4) and concentrated in vacuo to afford 0.91 g (75% yield) of the title compound. 1H NMR (400 MHz, CDCl3) δ ppm 7.26-7.35 (5H, m), 3.59 (2H, s), 3.44-3.55 (4 H, m), 3.06 (2 H, dt, J=10.6, 1.8 Hz), 1.88-1.98 (2 H, m), 1.79-1.86 (1 H, m), 1.68 (3 H, m). LCMS (+ESI, M+H+) m/z: 236.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129398B2
Source datasetuspto-grants-2012_03
ORD IDord-bd6eaa30b1954179b5293953b1011631
Source noteuspto-grants-2012_03