HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-(1-Benzothiophen-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-(Chloromethyl)-1-benzothiophene | HCID 12813837 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 2-(1-Benzothiophen-2-yl)acetonitrile | HCID 12631923 | — |
Reaction Steps
To a solution of 2-chloromethyl-benzo[b]thiophene (1 eq.) in dioxane/water (2/1) was added KCN (1.5 eq.). The reaction was refluxed for 4 h. The crude was partitioned between water and EtOAc. The organic layer was washed with water, then brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc: 95/5 to 90/10) to afford benzo[b]thiophen-2-yl-acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759334B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-0ee2a227619148bfab509a57eefae68e |
| Source note | uspto-grants-2014_06 |