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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709698Generated: October 30, 2026

2,6-Dichloro-4-nitroaniline → HCID 23036559, compound

https://huagongshe.com/reaction/1709698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-4-nitroanilineHCID 7430—
ReactantSulfuryl chlorideHCID 24648—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 620617HCID 620617—
SolventDiethyl EtherHCID 3283—
ProductHCID 23036559HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950678
Source datasetuspto-grants-1990_08
ORD IDord-c48ea3a39766473cb70c6599afeadc61
Source noteuspto-grants-1990_08