HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Chloro-2-(4-chlorophenyl)-5-trifluoromethyl)-1H-pyrrole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile | HCID 11000143 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Chloro-2-(4-chlorophenyl)-5-trifluoromethyl)-1H-pyrrole-3-carbonitrile | HCID 178718 | 84% |
Reaction Steps
A mixture of 2-(p-chloropheny1)-5-(trifluoromethyl)pyrrole-3-carbonitile (8.12 g, 0.03 mol) and sodium acetate (0.25 g, 0.003 mol) in acetic acid at 70° C. is treated dropwise with bromine (0.48 g, 0.003 mol). When the color has disappeared, the reaction mixture is treated dropwise with sulfuryl chloride (6.1 g, 0.045 mol) over a 1 hour period, held at 70° C. for 1 hour, concentrated in vacuo and diluted with water. The reaction mixture is filtered, the filter cake is washed with water and dried to yield the title product as a white solid, 7.7 g (84% yield), mp 242°-243° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05449789 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-228cc80bc8ba410d9cda243787e60908 |
| Source note | uspto-grants-1995_09 |