Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate | HCID 53440113 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 3-(4-Nitrophenyl)pyrrole | HCID 21413421 | 26.9% |
Reaction Steps
A solution of 55 (2.44 g, 9.92 mmol) in ethylene glycol (25 mL) was flushed with argon for 20 min. The mixture was immersed in an oil bath pre-heated to 160° C., and powdered NaOH (4.22 g, 105 mmol) was added. Stirring was continued for 1.5 h. The reaction mixture was allowed to cool to room temperature, and water and CH2Cl2 were added. The aqueous layer was extracted with CH2Cl2. The organic extract was washed with water and brine. The organic layer was dried (Na2SO4). The solvent was removed at reduced pressure to yield a pale brown oil (502 mg, 25%): 1H NMR δ 6.36-6.48 (m, 1H), 6.69-6.73 (m, 2H), 6.79-6.81 (m, 1H), 6.96-6.98 (m, 1H), 7.33-7.38 (m, 1H), 8.21 (br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207329B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-7524f10eecfe4d8ab85352ab422caf04 |
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| Source note | uspto-grants-2012_06 |
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