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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167701Generated: October 31, 2026

Tetrahydrofuran → 1-Benzyl-4-methylpiperidin-4-ol

https://huagongshe.com/reaction/1167701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Benzyl-4-piperidoneHCID 19220—
Product1-Benzyl-4-methylpiperidin-4-olHCID 1084591359%

Reaction Steps

To a solution of 1-benzyl-4-piperidone (5.6 mL, 30.0 mmol) in 50 mL THF was added a solution of methyl]ithium in THF (24.0 mL, 36 mmol) dropwise at 0° C. over 15 min. The reaction mixture was allowed to warm to room temperature over 3 h and then quenched with 30 mL of sat. NH4Cl solution. The organic layer was extracted with diethyl ether (2×100 mL) and the combined organic layer was washed with brine (100 mL). The organic layer was separated, dried over Na2SO4, filtered and the solvent was removed in vacuo to obtain yellow gum. It was purified by column chromatography over silica gel with 9:1 EtOAc-MeOH as the eluting system to obtain 1-benzyl-4-methyl-4-piperidinol as a yellow thick oil (3.6 g, 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620815B1
Source datasetuspto-grants-2003_09
ORD IDord-e1e2b69755d64e40ad172a0b05cc4f0f
Source noteuspto-grants-2003_09