HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762769Generated: October 26, 2026
1-Bromooctane → 4-n-Octyloxy-4'-acetylbiphenyl
https://huagongshe.com/reaction/1762769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Acetoxy-4'-acetylbiphenyl | HCID 13531045 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | 4-n-Octyloxy-4'-acetylbiphenyl | HCID 14669759 | 75.8% |
Reaction Steps
4-Acetyloxy-4'-acetylbiphenyl (80.0 g, 0.315 mol) was suspended in ethylene glycol monoethyl ether (300 ml), followed by heating with stirring to obtain a uniform solution, pouring a 50% aqueous solution of KOH (70 g) therein, heating under reflux for 30 minutes, dropwise adding 1-bromo-n-octane (62.7 g, 0.325 mol), heating under reflux for 5 hours, cooling with air, pouring the solution on ice (1 l), extracting with toluene (2 l), washing the toluene layer with an acid, then with an alkali aqueous solution, further with water till the washing water became neutral, distilling off toluene for solidification, filtering on heating with toluene (1 l) and active carbon, and recrystallizing to obtain 4-n-octyloxy-4'-acetylbiphenyl (77.5 g). Yield: 75.71%. This product exhibited a smectic B liquid crystal phase (SB), and its C-SB point and SB-I point were 92.5° C. and 132.9° C., respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04834907 |
|---|
| Source dataset | uspto-grants-1989_05 |
|---|
| ORD ID | ord-d72f474d51944fc38d22bfec86b19478 |
|---|
| Source note | uspto-grants-1989_05 |
|---|