(1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Base Information

Chemical Name:(1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane
CAS No.:288102-57-8
Molecular Formula:C₁₇H₂₂BrNO₂
Molecular Weight:352.271
Hs Code.:

Synonyms:(1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Suppliers and Price of (1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

There total 2 articles about (1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 98-88-4
benzoyl chloride

: 288102-44-3
(1S,2S,4S,5R,10R/S)-2-hydroxymethyl-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

: 288102-57-8
(1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 14h;
DOI:10.1021/jo9919815

Reference yield:

: (2S,4S,5R)-2-hydroxymethyl-5-vinylquinuclidine

: 288102-57-8
(1S,2S,4S,5R,10R/S)-2-(benzoyloxymethyl)-5-(10-bromoethyl)-1-azabicyclo[2.2.2]octane

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / aq. HBr / 96 h / 20 °C

2: 88 percent / Et₃N / CH₂Cl₂ / 14 h / 20 °C

With hydrogen bromide; triethylamine; In dichloromethane; 1: Addition / 2: Acylation;
DOI:10.1021/jo9919815