HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → Methyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,4-Difluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoic acid | HCID 21074292 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoate | HCID 58781115 | — |
Reaction Steps
To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-nitro-benzoic acid (595.3 g, 1.363 mol) in acetone (9 L) was added sodium bicarbonate (609.0 g, 3.48 mol) and the mixture was stirred for 10 min. To this suspension was added dimethylsulfate (285.6 ml, 3.026 mol) and refluxed for 3 h (completion of reaction was confirmed by TLC-hexane: EtOAc/4:1), cooled to room temperature and evaporated under vacuum. The residue (yellow) was further digested in hot methanol (2 L), filtered, washed with methanol and dried to give the title compound as a solid (yellow). Yield: 405.63g (65.54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160915B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-558c4bb42bc54c82a1524ebc74602d7d |
| Source note | uspto-grants-2007_01 |