HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → HCID 57744887, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67429515 | HCID 67429515 | — |
| Reactant | HCID 86617314 | HCID 86617314 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57744887 | HCID 57744887 | — |
Reaction Steps
Methyl 5-bromo-4-methyl-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate. At 0° C., DIEA (4.32 mL, 24.8 mmol) was added dropwise to a solution of methyl 3-amino-5-bromo-4-methylthiophene-2-carboxylate (6.20 g, 24.8 mmol) in DCM (100 mL), followed by dropwise addition of TFAA (3.45 mL, 24.8 mmol). The mixture was stirred at room temperature for 18 hours, diluted with CHCl3, washed with water, dried over MgSO4, and evaporated. The crude product was purified by flash chromatography using EtOAc/hexanes to give the title compound. MS (ESI) m/z: Calculated; 346.1: Observed; 345.9. 1H NMR (300 MHz, CDCl3) δ ppm 9.62 (1H, br. s.), 3.89 (3H, s), 2.15 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030346B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-f0067b49f5f34eaea57d9a9d18ff9677 |
| Source note | uspto-grants-2011_10 |