HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-acetyl-2-(3-bromo-4-nitro-1H-indazol-1-yl)acetohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 67259880 | HCID 67259880 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-acetyl-2-(3-bromo-4-nitro-1H-indazol-1-yl)acetohydrazide | HCID 70814862 | — |
Reaction Steps
A suspension of 2-(3-bromo-4-nitro-1H-indazol-1-yl)acetohydrazide (0.865 g) in anhydrous toluene (20 mL) was treated at ambient temperature with 1 equivalent of acetic anhydride. The reaction mixture was stirred at ambient temperature for 16 hours and concentrated under reduced pressure to afford the product (0.98 g) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841455B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-5b593553204646a98f22630dfcd0595c |
| Source note | uspto-grants-2014_09 |