Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328310Generated: October 25, 2026

Hydrochloric Acid → 4-Pentyl-4'-biphenylcarboxylic Acid

https://huagongshe.com/reaction/328310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromineHCID 24408—
ReactantHypobromous acidHCID 83547—
Reactant1-(4'-Pentyl-1,1'-biphenyl-4-yl)ethanoneHCID 5244416—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product4-Pentyl-4'-biphenylcarboxylic AcidHCID 206333584%

Reaction Steps

883 Gram of 4'-n-pentyl-4-acetylbiphenyl was introduced into a 30 l stainless steel reactor (provided with a stirrer, a reflux condenser and a funnel for dropwise adding), added 3.75 l of p-dioxane and dissolved with stirring. On the other hand, 1.8 kg of bromine was dropwise added to and dissolved in a solution of 2 kg of sodium hydroxide dissolved in 7.5 l of water, cooled to 10°-15° C. The resulting hypobromous acid solution was maintained at about 10° C. This solution was dropwise added to the above-mentioned p-dioxane solution over 50 minutes, followed by stirring at 35°-40° C for 3 hours, allowing to stand over one night, adding 250 g of sodium bisulfite, stirring, neutralizing with 2.8 l of conc. hydrochloric acid, separating the resulting solid by filtration, water-washing, drying and recrystallizing from 6 l of acetic acid, to give 747 g of 4'-n-pentyl-4-biphenylcarboxylic acid of m.p. 177° C (smectic liquid crystal being formed) (Yield 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017416
Source datasetuspto-grants-1977_04
ORD IDord-9189d12394724e63af70ab32205fe0ba
Source noteuspto-grants-1977_04