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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345479Generated: October 30, 2026

Potassium Iodide → 4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidineheptanoic acid ethyl ester

https://huagongshe.com/reaction/345479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 7-bromoheptanoateHCID 122490—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
SolventDimethylformamideHCID 6228—
Product4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidineheptanoic acid ethyl esterHCID 5406906687%

Reaction Steps

This compound was prepared according to the procedure used in Example 7. A mixture of 4.6 g (0.015 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.6 g (0.015 mole) of ethyl 7-bromoheptanoate, 6.4 g (0.061 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 50 ml of N,N-dimethylformamide gave 6.0 g of a dark oil. The oil was purified by high pressure liquid chromatography (Waters Associates Prep LC/System 500A; PrepPAK® 500/silica; ethyl acetate; flow rate 150 ml/min). The fractions containing the desired product were combined and concentrated under reduced pressure to yield 2.5 g (44%) of a viscous, yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057524
Source datasetuspto-grants-1991_10
ORD IDord-9c7064914503495f89defc295b079e3a
Source noteuspto-grants-1991_10