HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (4-Ethyl-1,3-thiazol-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | 2-Cyanoethanethioamide | HCID 1416277 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-Ethyl-1,3-thiazol-2-yl)acetonitrile | HCID 11701070 | 81.6% |
Reaction Steps
To a solution of 1-bromo-2-butanone (10.3 g, 57.98 mmol) in EtOH (200 mL) were added 2-cyanothioacetamide (5.8 g, 57.98 mmol) and triethylamine (1.59 mL, 11.6 mmol) and the solution was stirred under reflux for 1 h. After cooling down to r.t., the solvent was removed. The orange solid obtained was washed with AcOEt then cyclohexane, and recrystallized from EtOH to afford 7.2 g of the title compound as orange needles (Y=81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465736B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-4d7fa44a3fae490a8bc142800f35428d |
| Source note | uspto-grants-2008_12 |