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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,5-Trichloronitrobenzene | HCID 6983 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 3-((4,5-Dichloro-2-nitrophenyl)amino)-1-propanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04110333 |
|---|
| Source dataset | uspto-grants-1978_08 |
|---|
| ORD ID | ord-9373bc7db1ea40c2892ae46e72ed3ade |
|---|
| Source note | uspto-grants-1978_08 |
|---|