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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420292Generated: November 3, 2026

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

https://huagongshe.com/reaction/2420292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrichloronitrobenzeneHCID 6983—
Reactant3-Amino-1-propanolHCID 9086—
ReactantPotassiumHCID 5462222—
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 iodic and 200 parts of butanol is stirred and refluxed overnight. The butanol is removed be evaporated 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 trichoromethane and 5% of methanol as elluent. 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 numberUS04110333
Source datasetuspto-grants-1978_08
ORD IDord-9373bc7db1ea40c2892ae46e72ed3ade
Source noteuspto-grants-1978_08