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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1405392Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1405392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt3-IodooxetaneHCID 13356686—
Edukt(4-Cyano-2-methyl-phenyl)boronic acidHCID 16218401—
KatalysatorNickel(II) iodideHCID 26038—
Katalysator(1S,2S)-2-Aminocyclohexanol hydrochlorideHCID 11715205—
LösungsmittelEthanolHCID 702—
LösungsmittelIsopropanolHCID 3776—
Produkt3-Methyl-4-(oxetan-3-YL)benzonitrileHCID 6815330965,42%

Reaktionsschritte

(4-Cyano-2-methyl-phenyl)boronic acid (1.75 g, 10.87 mmol), diiodonickel (102 mg, 0.326 mmol), (1S,2S)-2-aminocyclohexan-1-ol hydrochloride (50 mg, 0.33 mmol) and NaHMDS (2.01 g, 11.0 mmol) were combined in isopropanol (10 mL) under N2 in a pressure vial. A solution of 3-iodooxetane (1.00 g, 5.44 mmol) in isopropanol (1 mL) was added. The vial was immersed in a pre-heated 90° C. oil bath and stirred for 2 h, then cooled, diluted with ethanol (20 mL), filtered over Celite, concentrated, then absorbed onto Celite and purified by silica gel column chromatography (0-60% EtOAc/hexane) to give 3-methyl-4-(oxetan-3-yl)benzonitrile (616 mg, 3.556 mmol, 65.42%) 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
PatentnummerUS08916565B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-e1140e27dd8b4332a0632d541dab42c0
Quellennotizuspto-grants-2014_12