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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1458893생성일: 2026년 10월 26일

Chlorotrimethylsilane → N,N-Diethyl-6-diphenylmethyl-5,5-ethylenedioxy-1-azabicyclo-[2.2.2]octane-3-carboxamide

https://huagongshe.com/reaction/1458893

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참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctaneHCID 81858—
반응물N,N-diethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]octane-3-carboxamideHCID 21862301—
용매Ethylene GlycolHCID 174—
생성물N,N-Diethyl-6-diphenylmethyl-5,5-ethylenedioxy-1-azabicyclo-[2.2.2]octane-3-carboxamideHCID 5363346888.5%

반응 조건

온도100 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05852038
출처 데이터셋uspto-grants-1998_12
ORD IDord-6a46400dfc3845c4baf93917236efac7
출처 메모uspto-grants-1998_12