HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-(i-Propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | 4-(Thiophen-3-yl)aniline | HCID 4130336 | — |
| Reactant | Methyl 3-(i-propylsulfonyl)-2-oxopropanoate | HCID 58365407 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(i-Propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-one | HCID 58365316 | 79% |
Reaction Steps
A mixture of methyl 3-(i-propylsulfonyl)-2-oxopropanoate (0.23 g, 1 mmol), 4-thiophene-3-ylaniline (0.18 g, 1 mmol), 2-methoxybenzaldehyde (0.14, 1 mmol), acetic acid (0.023 mL, 0.4 mmol) and toluene (3 mL) was heated at reflux overnight. After the reaction was completed, the reaction mixture was allowed to cool to room temperature. To the mixture was added ether and precipitated compound was collected by filtration. The resulting aimed compound was washed with ether/n-hexane solution to give 4-(i-propylsulfonyl)-3-hydroxy-1-(4-thiophene-3-ylphenyl)-5-(2-methoxyphenyl)-1,5-dihydropyrrole-2-one (0.37 g, yield: 79%) as pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575197B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-b602de288ce0466ebacf50b38907cb85 |
| Source note | uspto-grants-2013_11 |