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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Hypobromous acid | HCID 83547 | — |
| Reactant | 1-(4'-Pentyl-1,1'-biphenyl-4-yl)ethanone | HCID 5244416 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Pentyl-4'-biphenylcarboxylic Acid | HCID 2063335 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04017416 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-9189d12394724e63af70ab32205fe0ba |
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| Source note | uspto-grants-1977_04 |
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