3-formamido>quinuclidine

Base Information

Chemical Name:3-formamido>quinuclidine
CAS No.:150208-85-8
Molecular Formula:C₁₆H₂₀Cl₂N₂O
Molecular Weight:327.254
Hs Code.:

3-<N-<2-(3,4-dichlorophenyl)ethyl>formamido>quinuclidine

Synonyms:3-formamido>quinuclidine

Suppliers and Price of 3-formamido>quinuclidine

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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 3-formamido>quinuclidine

Chemical Property:

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Technology Process of 3-formamido>quinuclidine

There total 4 articles about 3-formamido>quinuclidine 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: 100.0%

: 150235-78-2
(1-Aza-bicyclo[2.2.2]oct-3-yl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine

: 109-94-4
formic acid ethyl ester

: 150208-85-8
3-formamido>quinuclidine

Guidance literature:: With formic acid; Heating;
DOI:10.1021/jm00068a007

Reference yield:

: 5807-30-7
3,4-dichlorophenyl acetic acid

: 150208-85-8
3-formamido>quinuclidine

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / DCC / CH₂Cl₂

2: AlH₃ / tetrahydrofuran / 20 h / Ambient temperature

3: 100 percent / HCOOH / Heating

With aluminium hydride; formic acid; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00068a007

Reference yield:

: 6530-09-2
3-aminoquinuclidine dihydrochloride

: 150208-85-8
3-formamido>quinuclidine

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / DCC / CH₂Cl₂

2: AlH₃ / tetrahydrofuran / 20 h / Ambient temperature

3: 100 percent / HCOOH / Heating

With aluminium hydride; formic acid; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00068a007