HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → Methyl 2-amino-3-iodo-5-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Methyl 2-amino-5-(trifluoromethyl)benzoate | HCID 14233808 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Methyl 2-amino-3-iodo-5-(trifluoromethyl)benzoate | HCID 118251642 | 68% |
Reaction Steps
A solution of methyl 2-amino-5-(trifluoromethyl)benzoate (0.59 g, 2.7 mmoles) in trifluoroacetic acid (5 ml) was treated with N-iodosuccinimide (0.68 g, 3.0 mmoles) and stirred at ambient temperature for 18 h. The mixture was evaporated to dryness and the residue treated with water (25 ml) and basified with potassium carbonate then extracted with dichloromethane (25 ml). The organic phase was then washed with 10% sodium metabisulphite solution (25 ml), separated and dried over sodium sulphate, filtered and evaporated to dryness. The residue was chromatographed on silica gel eluting with an ethyl acetate/isohexane gradient. This gave the title compound 2 as a white solid (0.633 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365569B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-f2d3700a8c664e86aa01a491d7fac35b |
| Source note | uspto-grants-2016_06 |