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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599787Generated: November 1, 2026

2-Bromoanisole → 4-(2-methoxyphenyl)piperidin-4-ol

https://huagongshe.com/reaction/1599787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanisoleHCID 11358—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(2-methoxyphenyl)piperidin-4-olHCID 1063213484.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 15 g of 2-bromoanisole in 50 ml of THF is cooled to -70° C., under nitrogen, a 1.6M solution of n-butyllithium in THF is added dropwise and the mixture is kept stirring for 1 hour. The mixture is cooled to -70° C. and a solution of 15.2 g of 1-benzylpiperid-4-one in 50 ml of THF is added dropwise. The mixture is kept stirring while allowing the temperature to rise to RT and after 1 hour, the reaction mixture is concentrated under vacuum. The residue is taken up in AcOEt, the organic phase washed with water, with a saturated solution of NaCl, dried over MgSO4 and the solvent evaporated under vacuum. 14 g of the expected product are obtained after crystallization from the AcOEt/ether/heptane mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05741910
Source datasetuspto-grants-1998_04
ORD IDord-840d6d1a52244f4281321b6e748312fb
Source noteuspto-grants-1998_04