HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → HCID 21466808, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 135976857 | HCID 135976857 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21466808 | HCID 21466808 | 83.8% |
Reaction Steps
To a solution 0.8 g of 6-decyl-2-(4-hydroxyphenyl)quinoline and 170 mg potassium hydroxide in i2 ml of butanol, 0.5 g of pentyl bromide was added, followed by heat refluxing for 4 hours. After the reaction, the reaction mixture was poured into water and subjected to extraction with toluene. The organic layer was washed with water, dried with anhydrous sodium sulfate and subjected to distilling-off of the solvent, followed by purification by silica gel column chromatography and recrystallization to obtain 0.8 g of 6-decyl-2-(4-pentyloxyphenyl)quinoline. This compound showed the following phase transition series.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05695684 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-dbc1e4ffd3624504aaa695558c0ca417 |
| Source note | uspto-grants-1997_12 |