HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-1-butanol → (s)-4-(6-Methyloctyloxy)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-1-butanol | HCID 8723 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | 1-Bromo-6-methyloctane | HCID 13548105 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (s)-4-(6-Methyloctyloxy)benzonitrile | HCID 54307675 | — |
Reaction Steps
Add 5.75 g of 4-cyanophenol 10 g of 1 brom-6-methyl octane synthesized of available active amyl alcohol, 6.67 g of anhydrous potassium carbonate, 30 ml of N,N-dimethyl formamide into 100 ml four-mouth flask under nitrogen atmosphere, allow to react for 8 hours at 110° C. After the reaction, filter the insoluble matter, then extract ether. The organic layer is then washed with 5% NaOH, water and saturated salt water, then dried and evaporated to remove the ether. Then when the obtained oily matter is refined, 11.4 g of optical (s)-4-(6-methyloctyloxy)benzonitrile is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04725688 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-097ce1f06049442d8b63f92135cc032e |
| Source note | uspto-grants-1988_02 |