HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643933Generated: October 31, 2026
Hydrochloric Acid → HCID 178526404, compound
https://huagongshe.com/reaction/643933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,4,N-trihydroxy-5-nitrobenzamide | HCID 86624019 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178526404 | HCID 178526404 | — |
Reaction Steps
Thionyl chloride (20 mL) is added dropwise to a mixture of 2,4,N-trihydroxy-5-nitrobenzamide (6.7 g, 31.3 mmol) in THF (500 mL). The mixture is allowed to come to reflux during the addition and then heated at 55° C. for 18 h. The mixture is allowed to cool to room temperature. The insoluble precipitate is filtered off and the filtrate is concentrated and stripped twice with toluene to a give 4-nitro-6-(2-oxo-[1,3,2,4]dioxathiazol-5-yl)-benzene-1,3-diol as a gummy solid. To a suspension of the solid in dioxane (100 mL) is added dropwise triethylamine (16.9 mL, 121 mmol). After stirring at room temperature for 45 min, ice and water are added and the mixture is acidified with 1N HCl. The mixture is extracted twice with EtOAc and the organic layers are washed with 1N HCl and brine, and dried over MgSO4, filtered and concentrated. The crude material is purified using flash chromatography on silica gel eluting with 1:1 EtOAc/hexanes to afford 5-nitrobenzo[d]isoxazole-3,6-diol as a yellow solid: (M−H)−=195.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07700633B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-5d14b683a22341eb97b4567d4d8b07c8 |
|---|
| Source note | uspto-grants-2010_04 |
|---|