HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Benzoic acid, 4-amino-2-chloro-5-iodo-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | Benzoic acid, 4-amino-2-chloro-5-iodo-, methyl ester | HCID 11839203 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzoic acid, 4-amino-2-chloro-5-iodo-, methyl ester | HCID 11839203 | — |
| Product | Methyl 4-amino-2-chloro-3-iodobenzoate | HCID 59625863 | — |
Reaction Steps
Methyl 4-amino-2-chloro-5-iodo-benzoate, 70n. To a suspension of compound 70m (1.18 g, 6.38 mmol) and CaCO3 (12.8 mmol, 1.28 g) in MeOH (13 mL) was added a solution of iodine monchloride (6.70 mmol, 1.09 g) in CH2Cl2 (6 mL) dropwise at room temperature. The resulting reaction mixture was stirred at room temperature for 1.5 h. The reaction mixture was concentrated and then partitioned between EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 20-25% EtOAc/hexanes) to provide methyl 4-amino-2-chloro-5-iodo-benzoate 70n as major the product and methyl 4-amino-2-chloro-3-iodo-benzoate 70o as the minor product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455476B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-e54b86242a4746faa63a87612ad05887 |
| Source note | uspto-grants-2013_06 |