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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420587Generated: October 28, 2026

Ammonia → 3-p-biphenylyl-butylamine. Hydrochloride

https://huagongshe.com/reaction/2420587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChlorideHCID 312—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
ReactantEisessig-JodwasserstoffHCID 18398580—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-p-Biphenylyl-3-hydroxy-butyric acid ethyl esterHCID 70597377—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-p-biphenylyl-butylamine. HydrochlorideHCID 70597440—

Reaction Steps

A solution of 23.9 g of 3-p-biphenylyl-butyramide [m.p. 156°- 158°' obtainable by Friedel-Crafts acetylation of biphenyl to give 4-acetylbiphenyl (m.p. 118°- 120°), reaction with bromoacetic acid ethyl ester/zinc to give 3-p-biphenylyl-3-hydroxy-butyric acid ethyl ester (m.p. 55°- 56°), treatment with HI/acetic acid, reaction of the resulting 3-p-biphenylyl-butyric acid (m.p. 118°- 12-°) with SOCl2 to give the chloride, and reaction with ammonia] in 500 ml of THF is added dropwise, while stirring, to a suspension of 7.6 g of LiAlH4 in 250 ml of absolute THF, the mixture is boiled for 16 hours, ethyl acetate is added, with cooling, followed by 32% sodium hydroxide solution and the mixture is worked up in the customary manner to give 3-p-biphenylyl-butylamine. Hydrochloride, m.p. 226°-228°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110447
Source datasetuspto-grants-1978_08
ORD IDord-5bcc1028357e424280765a2b3d77a06f
Source noteuspto-grants-1978_08