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HRID 713046Erstellt: 24. Oktober 2026

Sodium bis(trimethylsilyl)amide → 3-Methyl-4-(oxetan-3-YL)benzonitrile

https://huagongshe.com/de/reaction/713046

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt(1S,2S)-2-aminocyclohexanolHCID 7057408—
Edukt3-IodooxetaneHCID 13356686—
Edukt(4-Cyano-2-methyl-phenyl)boronic acidHCID 16218401—
KatalysatorNickel(II) iodideHCID 26038—
LösungsmittelEthanolHCID 702—
LösungsmittelIsopropanolHCID 3776—
Produkt3-Methyl-4-(oxetan-3-YL)benzonitrileHCID 681533091.084,7%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To (4-cyano-2-methyl-phenyl)boronic acid (1.75 g, 10.90 mmol), nickel iodide (0.10 g, 0.33 mmol), (1S,2S)-2-aminocyclohexan-1-ol (0.05 g, 0.33 mmol) and NaHMDS (2.01 g, 10.90 mmol) in isopropanol (10 mL) under an atmosphere of nitrogen was added 3-iodooxetane (1.00 g, 5.40 mmol) in isopropanol (1 mL) via cannula. The reaction mixture was heated at 90° C. for 2 hours, then cooled, diluted with ethanol (20 mL) and filtered over Celite®. The filtrate was concentrated in vacuo, then the residue was purified by silica gel column chromatography using 0-60% EtOAc/hexane as eluant to give 3-methyl-4-(oxetan-3-yl)benzonitrile (0.62 g, 65%) as a white solid. ESI-MS m/z calc. 173.1. found 174.3 (M+1)+; Retention time: 1.09 minutes (3 min run).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181273B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-6600768c72cc44b4a4faac589ed68567
Quellennotizuspto-grants-2015_11