HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229124Generated: October 30, 2026
5-Chloro-3-fluoro-2-phenylsulfinylpyridine → 5-Chloro-3-fluoro-2-(4-chloro-2-fluoro-5-methoxyphenyl)pyridine
https://huagongshe.com/reaction/2229124
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-3-fluoro-2-phenylsulfinylpyridine | HCID 18466522 | — |
| Reactant | HCID 178492975 | HCID 178492975 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-3-fluoro-2-(4-chloro-2-fluoro-5-methoxyphenyl)pyridine | HCID 18466521 | — |
Reaction Steps
A Grignard solution of 12.9 g (0.049 mol) of 4-chloro-2-fluoro-5-methoxyphenylmagnesium bromide in 60 ml of THF was added with stirring at 23-30° C. to a solution of 10 g (0.0392 mol) of 5-chloro-3-fluoro-2-phenylsulfinylpyridine in 150 ml of THF over a period of 10 min, and the mixture was stirred at 23° C. for another 4 h. The reaction mixture was concentrated under reduced pressure, taken up in methylene chloride and extracted in succession with 1 N hydrochloric acid, 1 N of aqueous sodium hydroxide solution and with water, and dried. The solution was filtered with suction through silica gel, concentrated, stirred with pentane, filtered off with suction and dried, affording 5.7 g (50.1% of theory) of the title compound of mp. 120-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420314B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-057a878196874b5daa16b9318765e5a7 |
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| Source note | uspto-grants-2002_07 |
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