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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476924Generated: October 30, 2026

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

https://huagongshe.com/reaction/476924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
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 1351996451%

Reaction Steps

To magnesium turnings (6.08 g, 0.25 mole) and an iodine crystal in 600 ml of dry tetrahydrofuran (THF) (distilled from lithium aluminum hydride) and under an atmosphere of nitrogen was added dropwise a solution of p-bromofluorobenzene in 125 ml of THF. The temperature of the reaction mixture was kept below 10° C. by cooling in an ice-methanol bath. The mixture was stirred at room temperature for 1.5 hr. A solution of 1-(phenylmethyl)-4-piperidinecarboxylic acid ethyl ester (24.7 g, 0.10 mole) in THF was added, and the mixture was stirred at room temperature for 17 hr. The reaction mixture was poured into an icy, aqueous solution of ammonium chloride, and the resulting solution was extracted with methylene chloride. The solution was extracted with dilute sodium hydroxide and was dried (magnesium sulfate). The solvent was removed in vacuo to give an oil. This was crystallized from ether-hexane to give 19.87 g (51%) of title compound, m.p. 113°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886794
Source datasetuspto-grants-1989_12
ORD IDord-299dd4a7b864443c8c9fa9d13b02ffc3
Source noteuspto-grants-1989_12