Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 5-bromo-3-methylthiophene-2-carboxylate | HCID 53438912 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 59144031 | HCID 59144031 | — |
Reaction Steps
In a 100 mL round bottom flask, methyl 5-bromo-3-methylthiophene-2-carboxylate (1.50 g, 6.38 mmol) was dissolved in tetrachloromethane (30 mL). To above solution was added 1-bromopyrrolidine-2,5-dione (1.14 g, 6.38 mmol, 1.0 eq) and diphenylperoxyanhydride (0.155 g, 0.638 mmol, 0.1 eq). The reaction was stirred at 90° C. for 18 hr. To above reaction was added dichloromethane (30 mL), washed with aqueous sodium bicarbonate, brine and water. The organic phase was dried over MgSO4, filtered and concentrated. The crude was used in next step without purification. LC-MS (IE, m/z): 337.4 [M+N]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09056859B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-992403816980471c944d15d5b797d91b |
|---|
| Source note | uspto-grants-2015_06 |
|---|