HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → (1,5-Dimethyl-1H-pyrrol-3-yl)(4-methylphenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (1,5-Dimethyl-1H-pyrrol-2-yl)(4-methylphenyl)methanone | HCID 12648628 | — |
| Product | (1,5-Dimethyl-1H-pyrrol-3-yl)(4-methylphenyl)methanone | HCID 12648631 | — |
Reaction Steps
A 1.0g sample of 1,2-dimethyl-5-p-toluoylpyrrole in 10g of dried p-toluenesulfonic acid heated at 105° C for 1 hour. The solution is then poured into sodium bicarbonate solution and extracted into chloroform. The chloroform is evaporated in vacuo and the residue is recrystallized from ethyl acetate to give 1,2-dimethyl-4-p-toluoylpyrrole as a tan solid; m.p. 117°-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002643 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-fb857c9ae75747ef8f872f0616f87a7a |
| Source note | uspto-grants-1977_01 |