HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 2,4,N-trihydroxy-5-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2,4-Dihydroxy-5-nitrobenzoyl chloride | HCID 86624018 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,4,N-trihydroxy-5-nitrobenzamide | HCID 86624019 | — |
Reaction Steps
A solution of 2,4-dihydroxy-5-nitrobenzoyl chloride (17.0 g, 78.1 mmol) in dioxane (70 mL) is added to an ice cold solution of 50% aqueous hydroxylamine (35 mL) and water (35 mL). After the addition is complete, the ice bath is removed and the mixture is stirred at room temperature for 30 min. The resulting thick precipitate is filtered, washed once with 1:1 water/dioxane and dried to obtain 2,4,N-trihydroxy-5-nitrobenzamide. After standing in the refrigerator for 18 h, the 1:1 water/dioxane solution affords additional 2,4,N-trihydroxy-5-nitrobenzamide: (M+H)+=215.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700633B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-7451c0f418a543ad859bd2aa406b2ed7 |
| Source note | uspto-grants-2010_04 |