HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate | HCID 66707189 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate | HCID 66707680 | 106.2% |
Reaction Steps
Bromine (0.56 ml, 11 mmol) was added to a solution of 1 g (5.3 mmol) of ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate (WO2006087543) and 0.8 ml (5.7 mmol) Et3N in CH2Cl2. After stirring at room temperature for 2 h, aqueous NaHSO3 was added and the CH2Cl2 was removed and the aqueous residue was partitioned between water and EtOAc. The EtOAc layer was separated and washed with brine. The EtOAc layer was dried over anhydrous MgSO4, and the solvent was removed to give 1.5 g of the product as a solid. MS (ES) (MH+): 240 for C8H9BrClNO2; NMR (d6-DMSO): 1.3 (t, 3H), 2.2 (s, 3H), 4.2 (q, 2H), 12.3 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071605B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-f8c919a1364e42e788a071f2188cd9ef |
| Source note | uspto-grants-2011_12 |