HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226084Generated: October 30, 2026
Sulfuric acid magnesium salt (1:1) → 3-Bromo-5-chlorothieno[3,2-b]pyridine
https://huagongshe.com/reaction/226084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Chlorothieno[3,2-b]pyridine | HCID 12415568 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-5-chlorothieno[3,2-b]pyridine | HCID 71464339 | 54.2% |
Reaction Steps
1.00 g of 5-Chloro-thieno[3,2-b]pyridine (5.91 mmol), 497 mg of sodium bicarbonate (5.91 mmol), 1.54 g of potassium hydrogenphosphate (8.87 mmol) and 1.07 g of magnesium sulfate (8.87 mmol) are placed in a flask with 50 ml of chloroform. The reaction mixture is stirred under reflux for 30 min. 0.55 ml of Bromine (10.82 mmol) is added and stirred under reflux overnight. 0.55 ml of Additional bromine (10.82 mmol) is added and stirred under reflux for 1 day. The reaction mixture is cooled to room temperature and water and CH2Cl2 are added. Organic layer is separated. The water layer is adjusted to pH=14 with 5N NaOH and extracted with CH2Cl2. All organic layers are combined together and dried over Na2SO4 and evaporated. The crude product is applied onto a silica-gel chromatography column (Hexane:AcOEt=5:1) to give 796 mg of the title compound (54%). 1H-NMR (CDCl3): 8.12 (d, 1H, J=7.9 Hz), 7.81 (s, 1H), 7.36 (d, 1H, J=7.9 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557103B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-a644666bc4fe44fcaa46dc18d521dacb |
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| Source note | uspto-grants-2009_07 |
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