HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1036868Erstellt: 25. Oktober 2026
Isobutylene → 2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile
https://huagongshe.com/reaction/1036868
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Isobutylene | HCID 8255 | — |
| Edukt | 3-Bromobenzaldehyde | HCID 76583 | — |
| Edukt | Ytterbium triflate | HCID 2733225 | — |
| Edukt | 4-Amino-3-methylbenzonitrile | HCID 7010316 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile | HCID 67289987 | 26,2% |
Reaktionsschritte
To a stirred solution of 4-amino-3-methyl-benzonitrile (10.3 g, 78.4 mmol) and 3-bromobenzaldehyde (9.2 mL, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 10-30% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (7.3 g, 26.1%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 355.0 & 357.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08546427B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-1d2e55a5f4514e8b9eb0a1c1afb69f7f |
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| Quellennotiz | uspto-grants-2013_10 |
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