HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 4-Chloro-3-cyanomethyl-5-methyl-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Bromomethyl-4-chloro-5-methyl-benzonitrile | HCID 67050496 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Chloro-3-cyanomethyl-5-methyl-benzonitrile | HCID 67050493 | 48% |
Reaction Steps
3-Bromomethyl-4-chloro-5-methyl-benzonitrile (0.9938 g, 4.06 mmol), potassium cyanide (0.529 g, 8.12 mmol) in ethanol (5.0 mL) and H2O (2.5 mL) was heated at 85° C. for 3 hr. The reaction mixture was cooled, diluted with ethyl acetate, washed with brine, dried (MgSO4), concentrated and purified by flash column chromatography (silica gel, 0 to 30% ethyl acetate/hexane) to give 4-chloro-3-cyanomethyl-5-methyl-benzonitrile as a white solid (0.3707 g, 48%). 1H NMR (300 MHz, CDCl3): 7.61 (s, 1H), 7.51 (s, 1H), 3.83 (s, 2H), 2.40 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334295B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-122627f21d7c456b9c24e131dddc5d7e |
| Source note | uspto-grants-2012_12 |