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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380237Generated: October 30, 2026

1-Bromo-4-fluorobenzene → alpha,alpha-Bis(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanol

https://huagongshe.com/reaction/1380237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 1-benzylpiperidine-4-carboxylateHCID 90423—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Productalpha,alpha-Bis(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanolHCID 13519964—

Reaction Steps

To a stirred and refluxing Grignard-complex, previously prepared starting from 70 parts of 1-bromo-4-fluorobenzene and 10 parts of magnesium in 270 parts of tetrahydrofuran, was added dropwise a solution of 25 parts of ethyl 1-(phenylmethyl)-4-piperidinecarboxylate in 90 parts of tetrahydrofuran. Upon completion, stirring was continued for 2 hours at reflux temperature. The reaction mixture was cooled and poured onto a saturate ammonium chloride solution. The organic phase was separated, dried, filtered and evaporated, yielding 40 parts of α,α-bis(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanol as a residue (intermediate 12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581171
Source datasetuspto-grants-1986_04
ORD IDord-c562ab325535482999366a885a0e5773
Source noteuspto-grants-1986_04