HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-(3-bromophenyl)-2,5-dimethyl-1H-pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Solvent | 2,5-Hexanedione | HCID 8035 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3-bromophenyl)-2,5-dimethyl-1H-pyrrole | HCID 4763654 | 96% |
Reaction Steps
A solution of 3-bromoaniline (2.50 mL, 23.0 mmol) in acetonylacetone (3.00 mL, 25.6, mmol) containing a small amount of p-TSA was heated at reflux in a round bottom flask fitted with a Dean Stark trap and a reflux condenser for 5 h. The reaction mixture was allowed to cool to rt and diluted with EtOAc. The solution was washed with 1N HCl and sat. NaHCO3 solution. The organic solutions were dried over Na2SO4, filtered, and concentrated to give the desired product as a light brown solid (5.5 g, 96%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652041B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-85da1545317a4534bbc5d18252565280 |
| Source note | uspto-grants-2010_01 |