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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417814Generated: November 2, 2026

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

https://huagongshe.com/reaction/1417814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-(4-methoxyphenyl)piperidin-4-olHCID 15907329—

Reaction Steps

4-Bromoanisole (13 ml, 0.1038 mol) in THF (13.5 ml) is added to a mixture of magnesium (2.24 g, 92.2 mmol) in dry THF (20 ml). When the magnesium is consumed the reagent mixture (XIII) is cooled in a ice/water bath and a mixture of 1-benzyl-4-piperidone (XII, 15 ml, 80.9 mmol) in THF (35 ml) is added dropwise over 21 minutes. The bath is then removed and the mixture stirred for 27 minutes, then poured into saturated aqueous sodium bicarbonate. The mixture is extracted several times with ether and the combined organic extracts are dried over magnesium sulfate, concentrated and the resulting material chromatographed on silica gel eluting with methanol/dichloromethane (4/96) containing ammonium hydroxide (0.4%). Impure fractions are combined and rechromatographed as above to give 1-benzyl-4-(4-methoxyphenyl)piperidin-4-ol (XIV), NMR (CDCl3) 1.74, 2.14, 2.46, 2.78, 3.58, 3.80, 6.88, 7.31 and 7.44 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877317
Source datasetuspto-grants-1999_03
ORD IDord-e9815747569f4ede9aa26e49515a0e41
Source noteuspto-grants-1999_03