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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704454Generated: November 3, 2026

Potassium Iodide → 3-((4,5-Dichloro-2-nitrophenyl)amino)-1-propanol

https://huagongshe.com/reaction/1704454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,4,5-TrichloronitrobenzeneHCID 6983—
Reactant3-Amino-1-propanolHCID 9086—
Solvent1-ButanolHCID 263—
Product3-((4,5-Dichloro-2-nitrophenyl)amino)-1-propanolHCID 112955—

Reaction Steps

A mixture of 113.2 parts of 1,2,4-trichloro-5-nitrobenzene, 75 parts of 3-amino-1-propanol, 0.2 parts of potassium iodide and 200 parts of butanol is stirred and refluxed overnight. The butanol is removed by evaporation in vacuo and water is added to the residue. The product is extracted with 4-methyl-2-pentanone. The extract is washed a few times with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is triturated in 2,2'-oxybispropane. The product is filtered off and crystallized from a mixture of 2,2'-oxybispropane and 2-propanol, yielding 31.7 parts of 3-[(4,5-dichloro-2-nitrophenyl)amino]-1-propanol; mp. 97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126687
Source datasetuspto-grants-1978_11
ORD IDord-c25e9cb369e445d582d86c3db8815ff5
Source noteuspto-grants-1978_11