HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70497Erstellt: 24. Oktober 2026
Ammonium Chloride → (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol
https://huagongshe.com/de/reaction/70497
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 4-Bromothioanisole | HCID 66037 | — |
| Edukt | 5-Chloro-6-methoxypicolinaldehyde | HCID 58452846 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol | HCID 67396108 | 72,3% |
Reaktionsschritte
n-Butyllithium (2.64 M, 2.9 mL) was added to a solution of 4-bromothioanisole (1.61 g) in tetrahydrofuran (20 mL) at −78° C. in a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (1.14 g) in tetrahydrofuran (10 mL) was added to the reaction solution, followed by stirring for one hour. The reaction solution was poured into a saturated ammonium chloride solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1→4:1) to give (5-chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol as a pale yellow oil (1.42 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822503B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-f806ee9f51c84a7e8397092246675d0c |
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| Quellennotiz | uspto-grants-2014_09 |
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