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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491690Generated: October 25, 2026

Methane → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanol

https://huagongshe.com/reaction/1491690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant[2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanoneHCID 9842862—
ReactantHCID 178506676HCID 178506676—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexane diethyletherHCID 21895417—
Productalpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanolHCID 18930344—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone (2.0 g, 5.26 mmol) in anhydrous tetrahydrofuran (50 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, phenyllithium (3.16 mL of a 2.0M solution in cyclohexane/ethyl ether, 6.31 mmol). Stir at -78° C. for 30 minutes, 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 (75% ethyl acetate/hexane) to give a yellow oil. Dissolve the oil in methylene chloride and treat with activated charcoal. Filter and evaporate the solvent in vacuo to give the title compound as a white electrostatic powder; mp 67°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371093
Source datasetuspto-grants-1994_12
ORD IDord-0d0604226d51409ea9040db17bf6b9b0
Source noteuspto-grants-1994_12