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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59746Generated: October 25, 2026

Sulfamic Acid → 5-Nitro-2-thenoic acid

https://huagongshe.com/reaction/59746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantEthyl AcetateHCID 8857—
Reactant5-Nitrothiophene-2-carboxaldehydeHCID 78281—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-Nitro-2-thenoic acidHCID 80591193.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5-nitrothiophene-2-carbaldehyde (1.685 g, 10.72 mmol) and sulfamic acid (1.249 g, 12.87 mmol) in dioxane (30 ml) was cooled to 0° C., and a solution of sodium chlorite (1.940 g, 21.44 mmol) in water (14 ml) was added drop-wise. The mixture was allowed to warm to RT and stirred for 2 hours. A second batch of 5-nitrothiophene-2-carbaldehyde (1.966 g, 12.51 mmol) was reacted under the same conditions using the molar ratios described above. The two reaction mixtures were combined and portioned between ethyl acetate and water. The organic layer was extracted twice with 5% NaHCO3 and the organic phase was discarded. The basic aqueous phase was acidified with 2N HCl (pH=2) and extracted twice with ethyl acetate. The combined organic layers were washed with brine and dried over sodium sulfate; the solvent was removed affording 5-nitrothiophene-2-carboxylic acid (Int. 53) (3.6 g, 20.79 mmol, MS/ESI+173.9 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440954B2
Source datasetuspto-grants-2016_09
ORD IDord-be9da77c97c64c5e89118dacb35a924e
Source noteuspto-grants-2016_09