Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobiphenyl | HCID 9461 | — |
| Reactant | 4-(4'-Fluoro-4-biphenylyl)-4-oxo-butyric acid | HCID 10730870 | — |
| Reactant | 4-(4'-Fluoro-4-biphenylyl)pentanoic acid amide | HCID 57072151 | — |
| Reactant | succinic anhydride AlCl3 | HCID 131711219 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Product | Eisessig-Jodwasserstoff | HCID 18398580 | — |
| Product | 4-(4'-Fluoro-4-biphenylyl)-4-hydroxy-pentanoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04239759 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-05f4d1aea5034d4c9f4eb4288a8de51d |
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| Source note | uspto-grants-1980_12 |
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