HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-{5-(2,4-dimethylbenzoyl)-1-methyl-1H-pyrrol-2-ylmethyl}nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| Reactant | 2,4-Dimethylbenzoyl chloride | HCID 140867 | — |
| Reactant | 4-(1-Methylpyrrol-2-ylmethyl)nitrobenzene | HCID 23285794 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 4-{5-(2,4-dimethylbenzoyl)-1-methyl-1H-pyrrol-2-ylmethyl}nitrobenzene | HCID 23285766 | 42.3% |
Reaction Steps
4-(1-Methylpyrrol-2-ylmethyl)nitrobenzene (1.2 g, 5.5 mmol) [prepared as in Example 7, Step (b)], 2,4-dimethylbenzoyl chloride (1.6 g, 9.5 mmol), and triethylamine (1.3 ml, 9.3 mmol) were dissolved in xylenes (50 ml), and the reaction mixture was heated at reflux under argon. After 48 h, the reaction mixture was passed through a Florisil® column (hexane followed by hexane-ethyl acetate, 95:5) to give 4-{5-(2,4-dimethylbenzoyl)-1-methyl-1H-pyrrol-2-yl-methyl}nitrobenzene (0.81 g, 42%) as a solid. ##STR41##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136844 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-c7829573583d4ad3b22599f3337920a0 |
| Source note | uspto-grants-2000_10 |