HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431765Generated: November 2, 2026
1,2-Dichloroethane → Benzoic acid, 3-(4-morpholinyl)-5-nitro-, 2-acetylhydrazide
https://huagongshe.com/reaction/1431765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59817793 | HCID 59817793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzoic acid, 3-(4-morpholinyl)-5-nitro-, 2-acetylhydrazide | HCID 67509241 | — |
Reaction Steps
A screw-cap vial was charged with 3-morpholino-5-nitrobenzoic acid (0.250 g, 0.991 mmol), sodium bicarbonate (0.250 g, 2.97 mmol), EDC (0.285 g, 1.487 mmol), 1-hydroxy-7-azabenzotriazole (0.202 g, 1.487 mmol), acetic hydrazide (0.088 g, 1.189 mmol), and DMF (2.0 mL). The orange solution was stirred at 23° C. for 18 h, then partitioned between EtOAc and water. The organic phase was washed with brine, dried over magnesium sulfate, and concd, affording N′-acetyl-3-morpholino-5-nitrobenzohydrazide as an orange oil. Mass Spectrum (ESI) m/e=309.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-57c3468c4dd3406684db0494e6cd921c |
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| Source note | uspto-grants-2015_01 |
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