HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1458893Erstellt: 26. Oktober 2026
Chlorotrimethylsilane → N,N-Diethyl-6-diphenylmethyl-5,5-ethylenedioxy-1-azabicyclo-[2.2.2]octane-3-carboxamide
https://huagongshe.com/reaction/1458893
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | 2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctane | HCID 81858 | — |
| Edukt | N,N-diethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]octane-3-carboxamide | HCID 21862301 | — |
| Lösungsmittel | Ethylene Glycol | HCID 174 | — |
| Produkt | N,N-Diethyl-6-diphenylmethyl-5,5-ethylenedioxy-1-azabicyclo-[2.2.2]octane-3-carboxamide | HCID 53633468 | 88,5% |
Reaktionsschritte
A mixture of (3R*, 4R*)-N,N-diethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]octane-3-carboxamide (10 g, 26 mmol), 1,2-bis(trimethylsiloxy)ethane (6 g, 29 mmol), trimethylsilyl chloride (20 ml) and ethylene glycol (50 ml) was heated at 100° C. for 3 hours. After by-products were removed by distillation 93° C./atmosphere pressure), the mixture was poured into cold aqueous sodium bicarbonate (NaHCO3) (250 ml) and extracted with methylene chloride (CH2Cl2) (100 ml) three times. The combined extracts were dried over sodium sulfate (Na2SO4) and concentrated. The clude was purified by recrystallization from ethyl acetate (EtOAc)/hexane to give 21 (1:2 mixture at 6-position; 23 mmol, 88%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05852038 |
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| Quelldatensatz | uspto-grants-1998_12 |
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| ORD ID | ord-6a46400dfc3845c4baf93917236efac7 |
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| Quellennotiz | uspto-grants-1998_12 |
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