HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 4-Cyclopropylcarbonylphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | (4-(Bromomethyl)phenyl)(cyclopropyl)methanone | HCID 15512829 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Cyclopropylcarbonylphenylacetonitrile | HCID 15512831 | — |
Reaction Steps
Mix (4-bromomethyl-phenyl)-cyclopropyl-methanone (5.0 g, 21 mmol), potassium cyanide (2.0 g, 30 mmol), tetra-butylammonium bromide (150 mg), water (5 mL) and acetonitrile (50 mL). Mechanically stir at room temperature for 3 hours, pour into water (450 mL) and stir overnight. Collect by filtration and recrystallize (hexane) to give the title compound as a white crystalline solid; mp 86-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479663B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-b7988ee3721149e3be397d4359f4fd43 |
| Source note | uspto-grants-2002_11 |