HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → ethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1H-Pyrrole-2-carboxylic acid, 3,5-dimethyl-, ethyl ester | HCID 137477 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylate | HCID 138486 | — |
Reaction Steps
To a solution of ethyl 3,5-dimethyl-1H-pyrrole-2-carboxylate (3.42 g, 20 mmol) in carbon tetrachloride (40 mL) was added a solution of bromine in carbon tetrachloride (10 mL) dropwise at 20° C. After the addition was complete, stirring was continued for 2 h. The reaction mixture was diluted with DCM, washed with aqueous NaHCO3 and water, and then dried over Na2SO4. Evaporation of solvent gave ethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylate as a solid (4.8 g), which was used in the next step without purification. 1H-NMR (CDCl3): δ 9.36 (1H, s), 4.30 (2H, q), 2.28 (3H, s), 2.26 (3H, s), 1.36 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026237B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c42fdd84f13e4bc9a801ccb67316cb09 |
| Source note | uspto-grants-2011_09 |