HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → (4-tert-Butylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene | HCID 87836 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-tert-Butylphenyl)acetonitrile | HCID 76784 | 115.6% |
Reaction Steps
4-t-Butylbenzylbromide (903 mg, 3.98 mmol) was reacted with NaCN (210 mg, 4.30 mmol) in ethanol (10 ml) and H2O (2 ml) at 80° C. The reaction solvent was removed in vacuo. The residue was diluted with EtOAc and H2O and the aqueous layer was extracted with EtOAc. The combined organic layer was dried over MgSO4 and then concentrated in vacuo. The residue was purified with column chromatography to yield title compound (797 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691855B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-08703d1572f24f2183bde874197ea58f |
| Source note | uspto-grants-2014_04 |