HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-Iodo-5-methyl-1H-benzoimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Methylbenzimidazole | HCID 11979 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-Iodo-5-methyl-1H-benzoimidazole | HCID 21886394 | 30.2% |
Reaction Steps
A solution of 5-methyl-1H-benzoimidazole (132 mg, 1.0 mmol) and NIS (248 mg, 1.10 mmol) in 1 mL of TFA was reflux for 1 hr and then cooled to RT. Treated with 30 mL of EtOAc, the mixture was neutralized with sat. NaHCO3 solution. The organic layer was washed with H2O (10 mL), brine (10 mL) and dried (Na2SO4). Removal of the solvent under reduced pressure followed by flash chromatography of the residue on silica gel (5% MeOH/CH2Cl2) gave 78 mg (30%) of product as a white solid: 1H-NMR (CDCl3; 400 MHz) δ 8.07 (d, 1H), 7.57 (br s, 1H), 7.22 (d, 1H, J. 8.4 Hz), 2.59 (s, 3H). Mass spectrum (ESI, m/z): Calcd. for C8H7IN2, 259.0 (M+H), found 259.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138530B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-ac87af7ff7c34219a70567ee909e8579 |
| Source note | uspto-grants-2006_11 |