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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193629Generated: October 31, 2026

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

https://huagongshe.com/reaction/1193629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1-(Phenylmethyl)-4-piperidinecarboxylic acid ethyl ester hydrochlorideHCID 70092284—
SolventTetrahydrofuranHCID 8028—
Productalpha,alpha-Bis(4-fluorophenyl)-1-(phenylmethyl)-4-piperidinemethanolHCID 1351996451%

Reaction Steps

To a 6.08 g (0.25 mole) of magnesium turnings and an iodine crystal in 600 ml of dry tetrahydrofuran and under an atmosphere of nitrogen was added, dropwise, a solution of p-bromofluorobenzene in 125 ml of tetrahydrofuran. The temperature of the reaction was kept below 10° C. by cooling in an ice-methanol bath. The mixture was stirred at room temperature for 1.5 hours. A solution of 24.7 g (0.10 mole) of 1-(phenylmethyl)-4-piperidinecarboxylic acid ethyl ester hydrochloride in tetrahydrofuran was added, and the mixture was stirred at room temperature for 17 hours. The reaction was poured into an icy, aqueous solution of ammonium chloride, and the resulting solution was extracted with methylene chloride. The methylene chloride solution was extracted with dilute sodium hydroxide and was dried over 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 the title compound, m.p. 113°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810713
Source datasetuspto-grants-1989_03
ORD IDord-0e74f6bea69e44e9b473a7cb314e57af
Source noteuspto-grants-1989_03