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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349256Erstellt: 25. Oktober 2026

Imidazole → (1,1-Dimethyl-2-nitro-ethoxy)-trimethyl-silane

https://huagongshe.com/reaction/349256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktDiethyl EtherHCID 3283—
EduktNitromethaneHCID 6375—
EduktChlorotrimethylsilaneHCID 6397—
Edukt1,1,3,3-TetramethylguanidineHCID 66460—
EduktTMS-ImidazoleHCID 14420972—
LösungsmittelAcetoneHCID 180—
LösungsmittelNitromethane acetoneHCID 18943953—
Produkt(1,1-Dimethyl-2-nitro-ethoxy)-trimethyl-silaneHCID 10899456—

Reaktionsschritte

To a solution of nitromethane (100 g, 1.64 mmol) and acetone (5 mL), add a catalytic amount of tetramethylguanidine. Using a syringe pump, add acetone (115 mL, 1.64 mmol) over a period of 72 h. to the stirred solution at RT. In a separate flask, combine chlorotrimethylsilane (206 mL, 1.64 mmol) and imidazole (123 g, 1.8 mmol) at 0° C. Transfer the nitromethane/acetone solution into the trimethylsilyl-imidazole mixture and allow the resulting mixture to stir 18 h at RT. Then cool the reaction to 0° C., dilute with cold ether (450 mL) and wash with cold 1N HCl (200 mL×2). Wash the organic layer with brine (300 mL). Carefully concentrate the crude material in vacuo without heating. Purify by distillation to provide the title compound. 1H NMR (300 MHz, CDCl3) δ 4.20 (s, 2H), 1.28 (s, 6H), 0.01 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179804B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-6208a9fba9df4033833b6ef4bea5b3a2
Quellennotizuspto-grants-2007_02