HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2,5-dimethyl-1-(4-ethoxyphenyl)pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | 4-Ethoxyaniline | HCID 9076 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,5-dimethyl-1-(4-ethoxyphenyl)pyrrole | HCID 846041 | — |
Reaction Steps
To a solution of acetonyl acetone (11.7 mL, 100 mmol) and toluene (750 mL) was added p-phenetidine (12.9 mL, 100 mmol) and glacial acetic acid (1 mL). The mixture was heated at reflux overnight. After cooling to rt, the mixture was concentrated in vacuo and purified by column chromatography on silica gel (15% EtOAc/hexanes) to give 2,5-dimethyl-1-(4-ethoxyphenyl)pyrrole as a pale yellow solid: 1H NMR (CDCl3, 500 MHz) δ 7.13-7.10 (m, 2H), 6.97-6.94 (m, 2H), 5.88 (br s, 2H), 4.08 (q, 2H), 2.02 (s, 6H), 1.46 (t, 3H); MS (ESI) 216 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465730B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-aad921157fae46d5987031026d18e8c8 |
| Source note | uspto-grants-2008_12 |