HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Methyl 5-(bromomethyl)-4-methylthiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl 4-methylthiophene-2-carboxylate | HCID 2777593 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(bromomethyl)-4-methylthiophene-2-carboxylate | HCID 67235212 | — |
Reaction Steps
To a solution of methyl 4-methylthiophene-2-carboxylate (2.7 g, 6.4 mmol) in dichloromethane (20 mL) is added 48% aq. HBr (12 mL), H2SO4 (6 mL), ZnBr2 (5.4 g), and HCHO (2.2 mL, 37%) at 0-5° C. The mixture is stirred at room temperature for 16 hours. The solution is diluted with water, extracted with dichloromethane, washed with NaHCO3 solution, saturated brine solution, water, dried over sodium sulfate, and concentrated to give the title compound as an off white solid (3.5 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822486B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-75a3a1029acb46478cf275d50c0806ed |
| Source note | uspto-grants-2014_09 |