HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4'-Hexyl[1,1'-biphenyl]-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (1,1'-Biphenyl)-4-carbonitrile, 4'-hexyl- | HCID 38764 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4'-Hexyl[1,1'-biphenyl]-4-carboxylic acid | HCID 13554588 | — |
Reaction Steps
5 Gram of 4-n-hexyl-4'-cyanobiphenyl, 40 ml of diethylene glycol, 4 ml of water and 2 g of sodium hydroxide were introduced into 200 ml three neck flask and heated with stirring for 25 hours, followed by acidifying with hydrochloric acid, separating by filtration and recrystallizing with glacial acetic acid to give 4.1 g of 4-n-hexyl-biphenyl-4'-carboxylic acid (II), which was a colorless crystal having a molecular formula of C19H22O2 (composition: C 80.8%, H 7.9%, O 11.3% as calculated values and C 80.4%, H 8.1%, O 11.5% as observed values) and a melting point of 170° -171° C and formed a smectic liquid crystal at temperatures exceeding the melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017416 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-baf99e0fdc284093a7109547019dea7d |
| Source note | uspto-grants-1977_04 |