HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → Methyl 2-amino-3-methyl-5-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | Methyl 2-amino-3-iodo-5-(trifluoromethyl)benzoate | HCID 118251642 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-amino-3-methyl-5-(trifluoromethyl)benzoate | HCID 118251663 | 96.1% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A mixture of methyl 2-amino-3-iodo-5-(trifluoromethyl)benzoate (0.633 g, 1.83 mmoles), trimethylboroxine (0.56 ml, 3.66 mmoles), cesium carbonate (1.2 g, 3.66 mmoles) and 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (0.075 g, 0.09 mmoles) in 1,4-dioxane (15 mL) was heated in a microwave reactor at 130° C. for 1.5 h. The mixture was partitioned between water (30 ml) and ethyl acetate (2×30 ml). The combined organics were 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 3 as an orange solid (0.41 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365569B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-b6cd06d9c0974345abc07764d824ba3d |
| Source note | uspto-grants-2016_06 |