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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733042Generated: November 1, 2026

4-Fluorobiphenyl → Eisessig-Jodwasserstoff

https://huagongshe.com/reaction/1733042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobiphenylHCID 9461—
Reactant4-(4'-Fluoro-4-biphenylyl)-4-oxo-butyric acidHCID 10730870—
Reactant4-(4'-Fluoro-4-biphenylyl)pentanoic acid amideHCID 57072151—
Reactantsuccinic anhydride AlCl3HCID 131711219—
ReactantHCID 178418373HCID 178418373—
ProductEisessig-JodwasserstoffHCID 18398580—
Product4-(4'-Fluoro-4-biphenylyl)-4-hydroxy-pentanoic acidHCID 20302408—

Reaction Steps

A solution of 27.1 g of 4-(4'-fluoro-4-biphenylyl)pentanoic acid amide [obtainable by reacting 4-fluorobiphenyl with succinic anhydride/AlCl3 to give 4-(4'-fluoro-4-biphenylyl)-4-oxobutanoic acid, reaction with CH3MgI to give 4-(4'-fluoro-4-biphenylyl)-4-hydroxy-pentanoic acid, dehydroxylation with HI/acetic acid to give 4-(4'-fluoro-4-biphenylyl)-pentanoic acid, conversion into the chloride employing SOCl2 and reaction with NH3 ] in 150 ml of dioxane is added dropwise at 0° to a solution of 24 g of bromine in 120 ml of 20% potassium hydroxide solution. The mixture is stirred for a further 1 hour, taken up in ether, the phases are separated and the organic phase is dried over sodium sulfate and evaporated. The crude product obtained is boiled for 20 hours with 60 g of KOH, 250 ml of methanol and 65 ml of water, in the course of which 3-(4' -fluoro-4-biphenylyl)-butyl-isocyanate, which is not isolated, is formed. After cooling, the mixture is worked up using water and ether to give 3-(4'-fluoro-4-biphenylyl)-butylamine, hydrochloride; m.p. 222°-224°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239759
Source datasetuspto-grants-1980_12
ORD IDord-05f4d1aea5034d4c9f4eb4288a8de51d
Source noteuspto-grants-1980_12