HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231734Erstellt: 25. Oktober 2026
Acetic Acid → 2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridine
https://huagongshe.com/reaction/231734
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-(3-Chlorophenyl)ethanone | HCID 14933 | — |
| Edukt | 3,3-Bis(methylsulfanyl)-1-phenylprop-2-en-1-one | HCID 280923 | — |
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridine | HCID 20031588 | — |
Reaktionsschritte
To 20 ml of tetrahydrofuran solution containing 0.69 g of m-chloroacetophenone was added 1.1 g of potassium t-butoxide at room temperature, followed by stirring for 30 minutes. Further, 1 g of 3,3-bis-(methylthio)-1-phenyl-2-propen-1-one was added, followed by stirring for 1 hour. Subsequently, 20 ml of acetic acid and 3 g of ammonium acetate were added, and reaction was carried out for 3 hours under reflux, while distilling away tetrahydrofuran. The reaction liquid was neutralized with an aqueous solution of sodium hydroxide, and the neutralized solution was extracted twice with 50 ml portions of ethyl acetate. The extract was dried with anhydrous magnesium sulfate. Ethyl acetate was distilled away under reduced pressure and the residues were recrystallized from isopropanol to give 1.1 g of 2-(3'-chloromethylphenyl)-4-methylthio-6-phenylpyridine. (m.p. 56.8° C.)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04849011 |
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| Quelldatensatz | uspto-grants-1989_07 |
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| ORD ID | ord-b0180c25d7db438096a5fdf4eb33bfd0 |
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| Quellennotiz | uspto-grants-1989_07 |
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