HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275294Generated: October 31, 2026
Quinoline → Ethyl 1,4 dimethyl-5-(rho-toluoyl)-pyrrole-2-acetate
https://huagongshe.com/reaction/1275294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Ethyl 3-carboxy-1,4-dimethyl-5-(p-toluoyl)-pyrrole-2-acetate | HCID 18424327 | — |
| Catalyst | HCID 178505374 | HCID 178505374 | — |
| Product | Ethyl 1,4 dimethyl-5-(rho-toluoyl)-pyrrole-2-acetate | HCID 18424313 | — |
Reaction Steps
A solution of 33.0 g. (0.096 mole) of ethyl 3-carboxy-1,4-dimethyl-5-(p-toluoyl)-pyrrole-2-acetate in 200 ml. of quinoline with 0.1 g. copper chromite added is heated under nitrogen for 6 hours at 200° C., then for 30 minutes at 220° C. The quinoline is distilled off in vacuo. The residue is dissolved in ether and washed successively with dilute hydrochloric acid, dilute sodium hydroxide, and brine; dried over magnesium sulfate; and the solvent evaporated in vacuo to give a brown oily residue which crystallizes. It is recrystallized from methanol, sublimed at 150° C. (0.025 mm/Hg) and recrystallized from hexane to give ethyl 1,4-dimethyl-5-(p-toluoyl)-pyrrole-2-acetate as a white solid, m.p. 90-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06160003 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-9ca4fe12717d468fac40b2fd8680bca0 |
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| Source note | uspto-grants-2000_12 |
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