HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl cyanide → 2-Hydroxy-2-(4-isobutylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Benzaldehyde, 4-(2-methylpropyl)- | HCID 577537 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Product | 2-Hydroxy-2-(4-isobutylphenyl)acetonitrile | HCID 19024787 | 107.5% |
Reaction Steps
Zinc iodide (0.21 g) was added to a mixture of 4-isobutylbenzaldehyde (6.5 g) and trimethylsilylcyanide (5.0 g). The mixture was stirred at room temperature for 3 minutes and partitioned between ethyl acetate and 7% hydrochloric acid. The organic layer was washed with 7% hydrochloric acid and water and dried over magnesium sulfate. The solvent was removed in vacuo to give 2-hydroxy-2-(4-isobutylphenyl)acetonitrile as a yellow oil (8.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212320 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-9efbf3dd78584800a75988f8512e6324 |
| Source note | uspto-grants-1993_05 |