Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 178444263 | HCID 178444263 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178444394 | HCID 178444394 | 21.1% |
Reaction Steps
First, 9.39 g of 4-(1-hydroxyethyl)-4′-(trans-4-pentylcyclohexyl)biphenyl, 0.52 g of potassium hydrogensulfate, and 50 ml of toluene were put in a 300 ml flask provided with a water content quantitative tube, and subjected to azeotropic dehydration under reflux for four hours. After the reaction, ether was added to the reaction solution, which was then washed with a saturated brine, and dried with sodium sulfate. The solvent was then distilled off. The residue was recrystallized from hexane to obtain 1.88 g (Y: 21.1%) of 4-(trans-4-pentylcyclohexyl)vinylbiphenyl. The purity of the resultant compound was 100.0% as measured by GC, 99.9% as measured by HPLC, and 1 spot as measured by TLC. The phase transfer temperature of the resultant compound was as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06388146B1 |
|---|
| Source dataset | uspto-grants-2002_05 |
|---|
| ORD ID | ord-ef0879f52ae94ea8b4fa3c32733240d0 |
|---|
| Source note | uspto-grants-2002_05 |
|---|