HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(beta-Hydroxyethyl)amino-4-(beta-hydroxyethyl)amino-6-(beta-hydroxyethyl)aminonitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 2-(beta-Hydroxyethyl)amino-6-(beta-hydroxyethyl)amino-4-chloronitrobenzene | HCID 20071091 | — |
| Product | 2-(beta-Hydroxyethyl)amino-4-(beta-hydroxyethyl)amino-6-(beta-hydroxyethyl)aminonitrobenzene | HCID 19851164 | — |
Reaction Steps
0.0072 mole (2 g) of 2-(β-hydroxyethyl)amino-6-(β-hydroxyethyl)amino-4-chloronitrobenzene, synthesized in stage 1 of example 2, was heated at 100°-110° C. with 6 ml of ethanolamine for 6 hours. The reaction medium was diluted with ice water then brought to neutrallity by addition of concentrated hydrochloric acid to precipitate out the desired product. After filtering and hot drying under vacuum in the presence of P2O5, it was recrystallized from 96° ethanol. It melted at 200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863482 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-392a6a096fe54f3890b1fdcbfecea432 |
| Source note | uspto-grants-1989_09 |