HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632328Generated: October 25, 2026
Sulfuric Acid → 2-(Ethyl(3-methyl-4-nitrosophenyl)amino)ethanol
https://huagongshe.com/reaction/1632328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(N-ethyl-m-toluidino)ethanol | HCID 7067 | — |
| Reactant | Isopropyl nitrite | HCID 10929 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Ethyl(3-methyl-4-nitrosophenyl)amino)ethanol | HCID 93929 | — |
Reaction Steps
360 g of N-ethyl-N-(2-hydroxyethyl)-m-toluidine and 1,250 g of water are initially introduced into a stirred flask. 196 g of concentrated sulfuric acid are added, while stirring and cooling. During this addition, the internal temperature should not rise above 50°. After cooling to 0°, 187 g of isopropyl nitrite is allowed to run in slowly at -2° to +2°. The excess of nitrite is then removed in the customary manner with amidosulfonic acid. The reaction mixture is brought to room temperature and degassed under reduced pressure. 60 g of prereduced Pd/C (5%) is added to this solution as the catalyst and the N-ethyl-N-(2-hydroxyethyl)-3-methyl-4-nitroso-aniline, which has not been isolated, is hydrogenated at 20° to 40° under a gauge pressure of 0.4 bar of hydrogen. When the reaction has ended, the reaction batch is let down, the catalyst is filtered off and the reaction mixture is concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474987 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-6ec3b9ecf7124b9a8a7a1c9b665877a8 |
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| Source note | uspto-grants-1984_10 |
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