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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181347Generated: November 5, 2026

5-Bromo-3-nitro-thiophene-2-carbaldehyde → 5-Bromo-3-nitrothiophene-2-carboxylic acid

https://huagongshe.com/reaction/1181347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-3-nitro-thiophene-2-carbaldehydeHCID 86247493—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product5-Bromo-3-nitrothiophene-2-carboxylic acidHCID 2994554580%

Reaction Steps

5Bromo-3-nitrothiophene-2-carbaldehyde (0.5953 g, 2.5012 mmol, prepared according to Sone, C; Matsuki, Y Bull Chem Soc Japan, 1963, 36(5), 618-20.) was dissolved in acetone (5 mL) and Jones Reagent (1.5 mL) was added. The reaction was stirred at RT for 1 h. The reaction was diluted with water (30 mL) and extracted with EtOAc (3×30 mL). The combined organics were washed With water (4×100 mL), dried over MgSO4 filtered and concentrated to give 0.4993 g (1.9892 mmol, 80%) of the product as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285557B2
Source datasetuspto-grants-2007_10
ORD IDord-3e7345aab5a9475e996762caf0632f32
Source noteuspto-grants-2007_10