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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1879458Erstellt: 25. Oktober 2026

Chlorotrimethylsilane → HCID 15281647, Verbindung

https://huagongshe.com/reaction/1879458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
Edukt(2S)-2-Amino-4,4-dimethylpentanoic acidHCID 194032—
EduktLithium borohydrideHCID 4148881—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 15281647HCID 1528164784,2%

Reaktionsschritte

To a stirred suspension of lithium borohydride (0.75 g, 34.4 mmol, 2.0 equiv.) in tetrahydrofuran (60 mL) was added trimethylsilyl chloride (7.48 g, 68.85 mmol, 4.0 equiv.) slowly over a period of 5 minutes at 0° C. under argon. To the reaction mixture was added (S)-2-amino-4,4-dimethyl-pentanoic acid (available from Chem-Impex International, Inc., Wood Dale, Ill., USA; 2.50 g, 17.2 mmol, 1.0 equiv.) in portions over a span of 10 minutes at the same temperature and the reaction was allowed to stir for 24 hours at room temperature. The reaction mixture was quenched with the slow addition of methanol (50 mL) at 0° C., and volatiles were removed by vacuum distillation. The obtained residue was treated with an aqueous solution of 20% potassium hydroxide (w/v; 10 mL) and extracted with dichloromethane (3×20 mL). The combined organic phases were dried over anhydrous sodium sulfate and concentrated under reduced pressure to give (S)-2-amino-4,4-dimethyl-pentan-1-ol (1.9 g, 84%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08314250B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-6d146d8749cf44688b1cadffb4cef64a
Quellennotizuspto-grants-2012_11