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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249641Generated: October 30, 2026

Potassium Hydroxide → Biphenyl

https://huagongshe.com/reaction/1249641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant[1,1'-Biphenyl]-4,4'-disulfonic acid, potassium salt (1:2)HCID 6096960—
SolventWaterHCID 962—
ProductBiphenylHCID 709595.7%

Reaction Steps

A 50% aqueous solution of potassium hydroxide and dipotassium 4,4'-biphenyldisulfonate were sent to a mixing tank 1 at a rate of 896 kg/hr and 390 kg/hr, respectively, and mixed with stirring. A hydrogenated triphenyl mixture was added to the resulting mixture in a dispersing tank 2 at a rate of 2900 kg/hr to disperse them. The dispersed mixture was dehydrated in a dehydrating tank 3, and then sent to a reservoir. From the reservoir 4, the dehydrated mixture of dipotassium 4,4'-biphenyldisulfonate, potassium hydroxide and hydrogenated triphenyl mixture was sent to a reaction tank 5 at a rate of 4190 kg/hr, and continuously reacted at 310° C. with a residence time of 6 hours in a nitrogen stream. After the reaction, the mixture was cooled by a heat exchanger 6, and sent to a water mixing tank 7 where it was mixed with 2000 liters/hr of water. Then, in a separating tank 8, the reaction medium layer was separated, and the aqueous layer was mixed with 45 kg/hr of activated tank in a mixing tank 9. The activated carbon was removed in a filtration device 10, and the residue was precipitated with dilute sulfuric acid in an acid precipitating tank 11. By separation in a centrifugal separator 12, 178 kg (yield 95.7%) of 4,4'-biphenyl was obtained hourly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04633024
Source datasetuspto-grants-1986_12
ORD IDord-971c6ea8d06640c488c8627cb708bd99
Source noteuspto-grants-1986_12