HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4'-(6-Hydroxyhexyloxy)-4-cyanobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Reactant | 4'-Hydroxy-4-biphenylcarbonitrile | HCID 140610 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4'-(6-Hydroxyhexyloxy)-4-cyanobiphenyl | HCID 11173950 | 43% |
Reaction Steps
To 800 ml of a methanol solution having dissolved therein 34 g (0.514 mol) of potassium hydroxide were added 100 g (0.512 mol) of 4-hydroxy-4'-cyanobiphenyl and 93 g (0.512 mol) of 6-bromo-1-hexanol, and the mixture was heated at reflux for 13 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate. The extract was concentrated under reduced pressure by the use of an evaporator, and the residue was purified by column chromatography using Wakogel C-200 as a carrier and hexane/THF, i.e., tetrahydrofuran as a developing solution to obtain 65 g (yield: 40%) of 4-(6-hydroxyhexyloxy)-4'-cyanobiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810433 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-9458846dff4d4869bec5e1a095016095 |
| Source note | uspto-grants-1989_03 |