HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → Ethyl 4-cyanophenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Thiobenzonitrile | HCID 585058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-cyanophenyl sulfide | HCID 21262891 | 83% |
Reaction Steps
Combine 4-mercapto-benzonitrile (0.4 g, 2.96 mmol), bromoethane (1.4 mL, 8.88 mmol) and potassium carbonate (3.3 g, 23.7 mmol) in anhydrous DMF (7 mL) and heat at 60° C. for 17 h. Cool the reaction mixture to ambient temperature and partition between brine (20 mL) and EtOAc (20 mL). Separate the organic layer, dry over anhydrous Na2SO4 and concentrate. Purify by chromatography on silica gel eluting with hexane/EtOAc (1:0, 9:1 and 4:1) to obtain the desired intermediate as a colorless oil (0.4 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022062B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c3aa0a5f7356458d8baf58e3291c277f |
| Source note | uspto-grants-2011_09 |