HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxybenzonitrile → 2-Hydroxy-5-iodo-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxybenzonitrile | HCID 11907 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Hydroxy-5-iodo-benzonitrile | HCID 7023040 | 81,626.898% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 2-hydroxy-benzonitrile (47.6 g, 0.400 mmol) in CH3CN (500 mL) was added CF3SO3H (40 mL) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 20 min, and then NIS (108 g, 0.48 mmol) was added. The mixture was stirred at room temperature overnight, then concentrated, diluted with H2O (300 mL) and extracted with EA (300 mL×3). Combined organic portions were dried over sodium sulfate, filtered and reconcentrated. Purification via column chromatography on silica gel (petroleum ether/ethyl acetate=5/1) afforded the title product (80 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975400B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-208cf829163a47fbb7e5f1681ca406b2 |
| Source note | uspto-grants-2015_03 |