HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 54555519, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | HCID 54420518 | HCID 54420518 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 54555519 | HCID 54555519 | 76.1% |
Reaction Steps
A mixture of the phenol prepared in example 91 (0.90 g, 2.2 mmol), 4-bromobutyronitrile (0.5 mL, 5.0 mmol), potassium carbonate (0.97 g, 7.0 mmol), potassium iodide (0.1 g) and methyl ethyl ketone (30 mL) was heated at reflux for 10 h. The reaction was concentrated in vacuo and the resulting residue partitioned between EtOAc and water. The layers were separated and the aqueous layer extracted with EtOAc (3×). The combined organic layers were washed with water (3×), brine, dried (MgSO4), and concentrated in vacuo to a light pink oil. The material was purified by flash chromatography over silica gel eluting with 5% MeOH/CHCl3 to provide 0.79 g (76%) of a clear oil. MS (FD+) 471.65. NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041684B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-48b0d9461283440d81c237e4255622a0 |
| Source note | uspto-grants-2006_05 |