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HRID 252683Erstellt: 26. Oktober 2026
2-Bromo-4,6-dimethylaniline → N-(2-Bromo-4,6-dimethylphenyl)(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl) dimethylsilanamine
https://huagongshe.com/reaction/252683
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Bromo-4,6-dimethylaniline | HCID 170579 | — |
| Edukt | Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane | HCID 58526148 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(2-Bromo-4,6-dimethylphenyl)(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl) dimethylsilanamine | HCID 58526146 | — |
Reaktionsschritte
Under and argon atmosphere, to a solution of 14.8 g (74.2 mmol) of 2-bromo-4,6-dimethylaniline in 200 ml of THF, 29.7 ml of 2.5 M (74.2 mmol) nBuLi in hexanes was added at −80° C. This mixture was warmed for ca. 1 hour to ambient temperature. Then, the resulting solution was added dropwise for ca. 1 hour while vigorously stirring to a solution of 18.0 g (74.2 mmol) of chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane in 100 ml of THF. The resulting mixture was stirred overnight at ambient temperature, then, evaporated to dryness. To the residue, 150 ml of toluene was added. This mixture was filtered through a glass frit (G4). The filtrate was evaporated to dryness. Fractional distillation gave a yellow liquid, bp 168-172° C./0.2 mm Hg. The product crystallizes slowly at ambient temperature. Yield 16.5 g (55%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07868197B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-35f68668ca2847aa9ae27e4f86ce4f4e |
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| Quellennotiz | uspto-grants-2011_01 |
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