HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944462Generated: November 1, 2026
3-Bromothiophene-2-carboxaldehyde → 3-(Pyridine-2-sulfonyl)thiophene-2-carbaldehyde
https://huagongshe.com/reaction/1944462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromothiophene-2-carboxaldehyde | HCID 2797079 | — |
| Reactant | Sodium Pyridine-2-sulfinate | HCID 23678794 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(Pyridine-2-sulfonyl)thiophene-2-carbaldehyde | HCID 86652188 | 6.4% |
Reaction Steps
A mixture of pyridine-2-sulfinate sodium salt (8.5 g), 3-bromothiophene-2-carbaldehyde (6.5 g) and dimethyl sulfoxide (50 mL) (split equally into four microwave vials) was heated by microwave irradiation at 125° C. for 45 minutes. The combined mixtures were diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by column chromatography on silica gel, eluting with a mixture of dichloromethane and ethyl acetate (1:0 to 0:1 by volume) to afford the title compound as a yellow solid (0.55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394836B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d9748e056adf4ca4a7766893eebf3c61 |
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| Source note | uspto-grants-2013_03 |
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