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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736450Generated: October 26, 2026

1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(thiophene-2-yl)-2-thiophenemethanol

https://huagongshe.com/reaction/1736450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl esterHCID 10869587—
ReactantHCID 178418439HCID 178418439—
SolventTetrahydrofuranHCID 8028—
Productalpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(thiophene-2-yl)-2-thiophenemethanolHCID 18930379—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve 1-[2-(4-methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester (4.0 g, 14.42 mmol) in anhydrous tetrahydrofuran (100 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, 2-lithiothiophene (14.42 mL of a 1M solution in tetrahydrofuran, 14.42 mmol) and stir at -78° C. for 3 hours. Add additional 2-lithiothiophene (14.42 mL of a 1M solution in tetrahydrofuran, 14.42 mmol) and stir at -78° C. for 2 hours. Remove the ice bath and allow to warm to room temperature. Quench with saturated ammonium chloride (100 mL), separate the organic phase and extract the aqueous phase with ethyl acetate. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (ethyl acetate) and recrystallize (ethyl acetate) to give the title compound as fluffy white crystals; mp 153°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541200
Source datasetuspto-grants-1996_07
ORD IDord-d9f1e054c8b74ba995c3394c9a2f349b
Source noteuspto-grants-1996_07