HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739648Generated: November 1, 2026
Phenylphosphonic dichloride → 5-Bromo-2-chloro-3-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/1739648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylphosphonic dichloride | HCID 69990 | — |
| Reactant | HCID 178517592 | HCID 178517592 | — |
| Product | 5-Bromo-2-chloro-3-(trifluoromethyl)pyridine | HCID 21836302 | — |
Reaction Steps
The product of Example 5 (11.5 g, 0.048 mol) and phenylphosphoryl dichloride (45 mL) were heated with stirring at 135° C. for four hours and allowed to cool to room temperature. The reaction mixture was poured onto ice (750 g) and allowed to warm to room temperature. The mixture was extracted with dichloromethane (150 mL) and filtered. The organic phase was separated, washed with water and 10% sodium carbonate solution and dried over anhydrous sodium sulphate. Evaporation of the solvent gave 2-chloro-3-trifluoromethyl-5-bromopyridine (11.6 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968875 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-bc1178f62f794614881bac365465cca1 |
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| Source note | uspto-grants-1999_10 |
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