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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 726827Erstellt: 26. Oktober 2026

Iodine → Methyl[(S)-2-methylbutyl]dichlorosilane

https://huagongshe.com/reaction/726827

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTrichloromethylsilaneHCID 6399—
EduktMagnesiumHCID 5462224—
Edukt1-Bromo-2-methylbutane, (+)-HCID 5464167—
Edukt(S)-(+)-1-Chloro-2-methylbutaneHCID 12431745—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktMethyl[(S)-2-methylbutyl]dichlorosilaneHCID 86751968—

Reaktionsschritte

Anhydrous tetrahydrofuran (125 mL) was put into a reactor with magnesium (9.5 g, 0.41 mol) and molecular sieves 4A which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. (S)-(+)-1-bromo-2-methylbutane (4.5 g, 0.03 mol) was added dropwise to the slowly stirred mixture. In addition, (S)-(+)-1-chloro-2-methylbutane (36 g, 0.34 mol) was added dropwise to the stirred mixture so that the reaction mixture was gradually refluxed. After the reaction was complete, the obtained Grignard reagent was transferred to a dropping funnel. The Grignard reagent was added dropwise to a solution being stirred containing methyltrichlorosilane (80 g, 0.54 mol) in anhydrous diethyl ether (150 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 2° C.-5° C. The reaction mixture was then stirred overnight at room temperature. Hexane (500 mL) was added to the reaction mixture, and the resulting mixture was filtered under pressure, followed by fractional distillation of the filtrate to provide the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05710301
Quelldatensatzuspto-grants-1998_01
ORD IDord-abb9039be0754379b37d48a9cf274a98
Quellennotizuspto-grants-1998_01