2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester

Base Information

Chemical Name:2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester
CAS No.:110589-97-4
Molecular Formula:C₈H₁₃NO₃
Molecular Weight:171.196
Hs Code.:
Mol file:110589-97-4.mol

Synonyms:2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester

Suppliers and Price of 2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester

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

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Chemical Property of 2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester

Chemical Property:

PSA：0.00000
LogP:0.00000

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester

There total 3 articles about 2-Oxa-3-azabicyclo[2.2.2]octane-3-carboxylic acid, methyl ester 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: 96.0%

: N-(carbomethoxy)-2-oxa-3-azabicyclo<2.2.2>oct-5-ene

: 110589-97-4
N-(carbomethoxy)-2-oxa-3-azabicyclo<2.2.2>octane

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; Ambient temperature;
DOI:10.1021/ja00257a037

Reference yield:

: 56239-25-9
2-Oxa-3-azabicyclo<2.2.2>oct-5-ene hydrochloride

: 110589-97-4
N-(carbomethoxy)-2-oxa-3-azabicyclo<2.2.2>octane

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / triethylamine / CH₂Cl₂ / 12 h

2: 96 percent / H₂ / 10percent Pd/C / ethyl acetate / Ambient temperature

With hydrogen; triethylamine; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1021/ja00257a037

Reference yield:

: 1165952-91-9
cyclohexa-1,3-diene

: 110589-97-4
N-(carbomethoxy)-2-oxa-3-azabicyclo<2.2.2>octane

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / diethyl ether; ethanol / 48 h / 5 °C

2: 55 percent / triethylamine / CH₂Cl₂ / 12 h

3: 96 percent / H₂ / 10percent Pd/C / ethyl acetate / Ambient temperature

With hydrogen; triethylamine; palladium on activated charcoal; In diethyl ether; ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/ja00257a037