HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1473402Erstellt: 25. Oktober 2026
Benzyl mercaptan → 6-(Benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazine
https://huagongshe.com/reaction/1473402
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl mercaptan | HCID 7509 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Edukt | 6-Bromo-1-chlorophthalazine | HCID 22030424 | — |
| Edukt | (2-Methoxy-4-(trifluoromethyl)phenyl)boronic acid | HCID 24901776 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Katalysator | HCID 178418807 | HCID 178418807 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 6-(Benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazine | HCID 86687448 | 43,1% |
Reaktionsschritte
A solution of 6-bromo-1-chlorophthalazine (0.500 g, 2.053 mmol), Pd2(dba)3 (0.047 g, 0.051 mmol), Xantphos (0.059 g, 0.103 mmol), and n,n-diisopropylethylamine (1.076 ml, 6.16 mmol) in 6 mL of dioxane was heated to 60° C. and was treated with benzyl mercaptan (0.243 ml, 2.053 mmol) drop wise. After stirring for one hour, LC/MS showed product and bis coupled product. (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid (0.407 g, 1.848 mmol), potassium carbonate (1.135 g, 8.21 mmol), PdCl2(dppf)-CH2Cl2 adduct (0.168 g, 0.205 mmol), and 2 mL of water were added and the reaction mixture was heated to 80° C. overnight. LC/MS showed mostly product, so the reaction mixture was allowed to cool to room temperature. The aqueous layer was removed, and the organics were concentrated. Purification of the crude residue by silica gel column chromatography (0 to 100% EtOAc/heptane) gave 6-(benzylthio)-1-(2-methoxy-4-(trifluoromethyl)phenyl)phthalazine (0.340 g, 0.797 mmol, 38.8% yield). m/z (ESI) 427.2 (M+H)+
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09012443B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-d9acc66ef21e415a80b17a51e6ebc392 |
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| Quellennotiz | uspto-grants-2015_04 |
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