HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048107Generated: November 2, 2026
Dibromodifluoromethane → HCID 58042418, compound
https://huagongshe.com/reaction/2048107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromodifluoromethane | HCID 6382 | — |
| Reactant | 2-Bromo-3-pyridinol | HCID 23070 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 58042418 | HCID 58042418 | 14% |
Reaction Steps
To a suspension of sodium hydride (1.72 g, 43.1 mmol) in NMP (50 mL) was added a solution of 2-bromo-3-hydroxypyridine (5 g, 28.74 mmol) in NMP (50 mL). This mixture was stirred at room temperature for 30 minutes followed by heating at 50° C. for 45 minutes before cooling to room temperature. Dibromodifluoromethane (3.15 mL, 34.5 mmol) was slowly added and the mixture was stirred at room temperature for 18 hours. The reaction mixture was slowly quenched into saturated aqueous ammonium chloride (100 mL) and extracted with EtOAc (3×100 mL). The combined organic extracts were washed with water (3×100 mL), brine (2×100 mL), dried over MgSO4 and concentrated in vacuo to afford a brown gum. This residue was purified using silica gel column chromatography eluting with 70/30 Heptane/EtOAc to give the title compound as a colourless oil (1.2 g, 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592629B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-669a78e12374417db32c257c53861251 |
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| Source note | uspto-grants-2013_11 |
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