HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid | HCID 21866991 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester | HCID 86596771 | 93% |
Reaction Steps
To a solution of 5-bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid (3) (4.50 g, 12.4 mmol) in a 3:1 mixture of THF:MeOH (32 mL) was added trimethylsilyldiazomethane (8.10 ml of a 2 M solution in hexanes) at room temperature. After stirring for 2 hours, the reaction mixture was quenched with acetic acid, diluted with EtOAc, and washed with water. The organic layer was dried (MgSO4) and concentrated under reduced pressure to give 4.35 g (93%) of the desired methyl ester (4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538120B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-6a6c031f93824f519437c591799bc5aa |
| Source note | uspto-grants-2009_05 |