HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → Benzo[b]thiophene-3-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3-(Chloromethyl)benzo(b)thiophene | HCID 76680 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Benzo[b]thiophene-3-acetonitrile | HCID 76681 | 65.9% |
Reaction Steps
To a stirred solution of NaCN (1.4 g, 28.5 mmol) in DMSO (8 mL) was added 3-(chloromethyl)-1-benzothiophene (4 gm, 21.9 mmol) in DMSO (6 mL) over 15 min. The reaction mixture was stirred at room temperature for 18 h and then quenched with water and extracted with ether (2×50 mL). The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography using ethyl acetate-hexane (1:1) to furnish 1-benzothien-3-ylacetonitrile (2.5 g, 65%). 1H NMR (200 MHz, CDCl3): δ 3.69 (s, 2H), 7.25-7.91 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772245B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9e9a173a102d4360b87ed539b30a777f |
| Source note | uspto-grants-2010_08 |