HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420097Erstellt: 25. Oktober 2026
Ammonium Chloride → 4-Bromo-1-isopropoxy-2-vinylbenzene
https://huagongshe.com/reaction/420097
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 5-Bromo-2-isopropoxybenzaldehyde | HCID 819973 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Methyl t-butylether hexane | HCID 21982663 | — |
| Produkt | 4-Bromo-1-isopropoxy-2-vinylbenzene | HCID 12542425 | 95% |
Reaktionsschritte
To a suspension of methyltriphenylphosphonium bromide (41.1 g, 115 mmol) in THF (1.2 L) cooled to −70° C., was added n-butyllithium (123 mmol, 2.5 M in hexanes). The mixture was stirred for a further 10 min, and then allowed to warm up to 0° C. and stir at this temperature for 10 min. The reaction mixture is then cooled again at −50° C., and 5-bromo-2-isopropoxybenzaldehyde (20.0 g, 82.2 mmol) in solution in THF (5 mL) was added. The mixture was stirred for 10 min, then allowed to warm up to room temperature. An ammonium chloride solution was added and the reaction mixture was diluted with a mixture methyl t-butylether/hexane, filtered through celite, and then dried over magnesium sulfate. The solvent was removed in vacuo to afford compound AY (18.9 g) as a pale yellow oil in 95% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093379B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-6acc623d9f0848d68c7d8795d896495e |
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| Quellennotiz | uspto-grants-2012_01 |
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