HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927574Generated: November 1, 2026
Hydrazine hydrate (1:1) → 3-Amino-2-hydroxy-N,N-dimethylbenzamide
https://huagongshe.com/reaction/1927574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-hydroxy-N,N-dimethyl-3-nitrobenzamide | HCID 11367803 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Acetic acid ethanol | HCID 18476134 | — |
| Product | 3-Amino-2-hydroxy-N,N-dimethylbenzamide | HCID 16098483 | — |
Reaction Steps
67.5 g of 2-Hydroxy-N,N-dimethyl-3-nitro-benzamide are dissolved in 1000 ml of EtOH/AcOH 9/1 and degassed 4× by evacuating and purging with argon. 7.5 g of Ru/C are added and the mixture obtained is degassed 4× by evacuating and purging with argon. A reaction mixture obtained is heated to reflux and 25 ml of hydrazine hydrate are added slowly. At 1 hour intervals 3 further portions of 25 ml of hydrazine hydrate are added. A reaction mixture obtained is cooled to rt, filtered and washed with EtOH. Solvent from the filtrate obtained is evaporated. Toluene is added 4× to the residue obtained and solvent is evaporated. A residue obtained is taken up in 1 l of H2O and 1 l of EtOAc. An aqueous layer obtained is extracted 3× with EtOAc. The organic layers obtained are washed 2× with brine, dried, filtered and solvent is evaporated. A residue obtained is purified by column chromatography over 500 g of silica using EtOAc/heptane 1/1 as the eluant to give 3-amino-2-hydroxy-N,N-dimethyl-benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08183281B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-1c2e42a6b8084ed3a90f004a53a93ce0 |
|---|
| Source note | uspto-grants-2012_05 |
|---|