HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936323Generated: October 25, 2026
Hydrochloric Acid → HCID 178444262, compound
https://huagongshe.com/reaction/1936323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 178444253 | HCID 178444253 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178444262 | HCID 178444262 | 46.7% |
Reaction Steps
First, 23.6 g of anhydrous aluminum chloride and 120 ml of methylene chloride were put in a 300 ml flask. After 14.0 g of acetyl chloride was dropped into the mixture at 5° C. or less, the resultant mixture was stirred keeping the same temperature for 30 minutes. Then, 45.2 g of 4-(trans-4-pentylcyclohexyl)biphenyl was added to resultant mixture at 5° C. or less and stirred for 30 minutes at room temperature. After the reaction, the reaction solution was poured into dilute hydrochloric acid, and an organic layer was separated. The organic layer was then washed with water and dried with sodium sulfate. The solvent was then distilled off. The residue was recrystallized from acetone to obtain 24.0 g (Y: 46.0%) of 4-acetyl-4′-(trans-4-pentylcyclohexyl)biphenyl. The purity of the resultant compound was 99.7% as measured by GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06388146B1 |
|---|
| Source dataset | uspto-grants-2002_05 |
|---|
| ORD ID | ord-c808bb0317524183bb7162557f29ab15 |
|---|
| Source note | uspto-grants-2002_05 |
|---|