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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazole | HCID 795 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Nitromethane | HCID 6375 | — |
| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Edukt | TMS-Imidazole | HCID 14420972 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Nitromethane acetone | HCID 18943953 | — |
| Produkt | (1,1-Dimethyl-2-nitro-ethoxy)-trimethyl-silane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07179804B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-6208a9fba9df4033833b6ef4bea5b3a2 |
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| Quellennotiz | uspto-grants-2007_02 |
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