HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-Bromobenzene-1-carbonyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Bromobenzoyl chloride | HCID 23542 | — |
| Product | 2-Bromobenzene-1-carbonyl cyanide | HCID 12969202 | 50% |
Reaction Steps
The reaction was carried out under Argon. Cuprous cyanide (6.52 g, 72.8 mmol) and anhydrous sodium iodide (20.25 g, 135 mmol) were stirred for 2 minutes in anhydrous acetonitrile (100 ml). The resulting solution was mixed with o-bromo benzoyl chloride (15.0 g, 68 mmol) whereupon an orange precipitate formed. The mixture was stirred for 30 minutes at room temperature, filtered and concentrated in vacuo. The residue was taken up in dichloromethane and the resulting precipitate was filtered off. Concentration of the filtrate under reduced pressure gave a yellow solid. Recrystallisation from 60°-80° C. b.p.t. petroleum ether afforded o-bromo benzoyl cyanide as yellow crystals (7.14 g, 50%), melting point 64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210312 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-9a11406d8d2f473788db22b1f38ae61f |
| Source note | uspto-grants-1993_05 |