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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111602Generated: October 30, 2026

4-Bromoanisole → 1-Benzyl-4-(4-methoxyphenyl)piperidin-4-ol

https://huagongshe.com/reaction/2111602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-Benzyl-4-(4-methoxyphenyl)piperidin-4-olHCID 1590732968.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 44.8 g of 1-bromo-4-methoxybenzene in 700 ml of THF is cooled to −78° C., 168 ml of a 1.6M solution of n-butyllithium in hexane are added dropwise and the mixture is then stirred at −78° C. for 30 minutes. The solution of 45.3 g of 1-benzyl-4-piperidinone in 100 ml of THF is then added dropwise and the mixture is stirred at −78° C. for 2 hours. The reaction mixture is poured into 400 ml of saturated NH4Cl solution and extracted with ether, the organic phase is washed with water, with saturated NaCl solution and dried over MgSO4, and the solvent is evaporated off under vacuum. 48.6 g of the expected product are obtained after crystallization from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521449B2
Source datasetuspto-grants-2009_04
ORD IDord-a34ac7fb7d234edf800463cc3dfa87d4
Source noteuspto-grants-2009_04