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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458893Generated: October 25, 2026

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

https://huagongshe.com/reaction/1458893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctaneHCID 81858—
ReactantN,N-diethyl-6-diphenylmethyl-5-oxo-1-azabicyclo[2.2.2]octane-3-carboxamideHCID 21862301—
SolventEthylene GlycolHCID 174—
ProductN,N-Diethyl-6-diphenylmethyl-5,5-ethylenedioxy-1-azabicyclo-[2.2.2]octane-3-carboxamideHCID 5363346888.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852038
Source datasetuspto-grants-1998_12
ORD IDord-6a46400dfc3845c4baf93917236efac7
Source noteuspto-grants-1998_12