HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254514Erstellt: 25. Oktober 2026
2-Bromobenzyl cyanide → 2-(2-Cyclopropylphenyl)acetonitrile
https://huagongshe.com/reaction/254514
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Bromobenzyl cyanide | HCID 29625 | — |
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | Tricyclohexylphosphine | HCID 75806 | — |
| Edukt | Cyclopropylboronic acid | HCID 2760897 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-(2-Cyclopropylphenyl)acetonitrile | HCID 58951775 | 63,6% |
Reaktionsschritte
To a solution of 0.784 g (4 mmol) 2-bromophenyl-acetonitrile in 16 ml toluene were added 0.8 ml water, 0.412 g (4.8 mmol) cyclopropylboronic acid, 2.97 g (14 mmol) tribasic potassium phosphate, 0.1 12 g (0.4 mmol) tricyclohexylphosphine and 0.045 g (0.2 mmol) palladium(II) acetate. The reaction mixture was stirred at 100° C. for 2 days. The solvent was evaporated and the residue taken up in water and ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was purified using column chromatography (SiO2, heptane/ethyl acetate 98:2) to yield 0.40 g of (2-cyclopropyl-phenyl)-acetonitrile as a light-yellow oil that was used directly for the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07875645B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-4d171b5178dd4365b39a40fdf193045c |
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| Quellennotiz | uspto-grants-2011_01 |
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