HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 5-ethyl-1H-pyrrole-2-carboxylate | HCID 597485 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 4-bromo-5-ethyl-1H-pyrrole-2-carboxylate | HCID 68580112 | 68% |
Reaction Steps
N-Bromosuccinimide (5.86 g, 0.033 mol) was added to a solution of ethyl 5-ethyl-1H-pyrrole-2-carboxylate (Intermediate 12, 5.0 g, 0.03 mol) in DCM (85 ml) at 0° C., and the reaction was stirred for 30 minutes then poured to a chilled beaker containing 2 N NaOH (50 ml). The layers were separated and the aqueous layer was extracted with DCM (×3). The combined organic extracts were washed with water and brine, dried over magnesium sulfate and concentrated. The resultant dark brown solid was purified by flash chromatography (hexanes/EtOAc, 10:1) to give the title product as a white solid (5.0 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709503B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e135598ffb5446758f60c3f60b9e7749 |
| Source note | uspto-grants-2010_05 |