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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193666Generated: November 2, 2026

Benzene, (3-bromopropoxy)- → HCID 23036406, compound

https://huagongshe.com/reaction/1193666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
ReactantSodium BicarbonateHCID 516892—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
Solvent1-ButanolHCID 263—
ProductHCID 23036406HCID 23036406—

Reaction Steps

A mixture of 3.37 g (0.011 mole) of [α,α-bis(p-fluorophenyl)]-4-piperidinemethanol, 2.52 g (0.011 mole) of (3-bromopropoxy)benzene and sodium bicarbonate (0.92 g, 0.011 mole) in 200 ml of 1-butanol was heated overnight to reflux. The butanol was removed by the rotary evaporator, and the residue partitioned between chloroform and water. Removal of the chloroform in vacuo gave a dark brown oil, the free base of the title compound. The base was converted to the oxalate salt and recrystallized from methanol-diethyl ether to give 1.41 g (23.9%) of white solid, m.p. 153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810713
Source datasetuspto-grants-1989_03
ORD IDord-d8740f4d690e4259a33309890413b7fd
Source noteuspto-grants-1989_03