HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dichloro-4-nitroaniline → HCID 23036559, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dichloro-4-nitroaniline | HCID 7430 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 620617 | HCID 620617 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23036559 | HCID 23036559 | — |
Reaction Steps
Sulfuryl chloride (4.68 g, 2.80 ml, 34.7 mmol) is added dropwise to 1-(2,6-dichloro-4-nitrophenyl)pyrrole (4.46 g, 17.4 mmol), prepared from 2,6-dichloro-4-nitroaniline and 2,5-dimethoxytetrahydrofuran following Example 12 procedures, in 20 ml of ether at 0°. After addition is completed, the mixture is stirred at RT for 60 hours. The reaction mixture is then poured into saturated aqueous sodium bicarbonate and extracted with ether. The combined organic layers are washed with brine, dried and stripped of solvent. The residue is purified by prep. TLC to give 2,5-dichloro-1-(2,6-dichloro-4-nitrophenyl)pyrrole, which is reduced with 16% aq. titanium(III) chloride to give 3,5-dichloro-4-(2,5-dichloro-1-pyrrolyl)aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04950678 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-c48ea3a39766473cb70c6599afeadc61 |
| Source note | uspto-grants-1990_08 |