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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643933Generated: October 31, 2026

Hydrochloric Acid → HCID 178526404, compound

https://huagongshe.com/reaction/643933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant2,4,N-trihydroxy-5-nitrobenzamideHCID 86624019—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178526404HCID 178526404—

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700633B2
Source datasetuspto-grants-2010_04
ORD IDord-5d14b683a22341eb97b4567d4d8b07c8
Source noteuspto-grants-2010_04