HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663266Generated: October 31, 2026
Hydrochloric Acid → [2,2'-Bithiophene]-5-carboxaldehyde
https://huagongshe.com/reaction/1663266
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2,2'-Bithiophene | HCID 68120 | — |
| Product | [2,2'-Bithiophene]-5-carboxaldehyde | HCID 364428 | 81% |
Reaction Steps
In a round bottom flask, phosphorus oxychloride (1.83 g) was added at 0° C. to 15 mL of DMF. After 30 minutes, 2,2′-bithiophene (500 mg) was further added and the solution stirred at room temperature for 30 minutes before heating to 50° C. until completion. Diluted hydrochloric acid was added at 0° C., the solution warmed to room temperature and the crude product extracted with ethyl acetate. Purification by flash chromatography (SiO2) yielded the title product as a light brown powder (81%). 1H-NMR (300 MHz, [D] acetone): δ=9.89 (s, 1H), 7.70 (d, 1H, 3J=3.9 Hz), 7.39 (d, 2H, 3J=4.3 Hz), 7.28 (d, 1H, 3J=3.9 Hz), 7.11 (t, 1H, 3J=4.4 Hz). 13C-NMR (50 MHz, [D] acetone): δ=183.0, 147.6, 142.1, 137.8, 136.5, 128.8, 127.5, 126.6, 124.7. EI-MS: m/z ([M]+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034895B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-a4522f0f1ff54259a4f5713f4b5d0a63 |
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| Source note | uspto-grants-2011_10 |
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