(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

Base Information

Chemical Name:(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride
CAS No.:1609286-15-8
Molecular Formula:C₁₃H₁₈ClN₂*Cl
Molecular Weight:273.205
Hs Code.:

Synonyms:(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

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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 (3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

Chemical Property:

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Technology Process of (3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

There total 6 articles about (3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride 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:

: 75-09-2
dichloromethane

: 1609286-14-7
(R)-2-phenyl-1,4-diazabicyclo[2.2.2]octane

: 1609286-15-8
(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: In acetone; at 20 ℃; for 336h;

Reference yield:

: 19883-41-1,13226-98-7
D-phenylglycine methyl ester hydrochloride

: 1609286-15-8
(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: Multi-step reaction with 6 steps

1: ammonium hydroxide / water; toluene / 24 h / 20 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Reflux

3: dmap; triethylamine / dichloromethane / 0 - 20 °C

4: borane-THF / tetrahydrofuran / 0 °C / Reflux

5: N,N-dimethyl-formamide / 12 h / 150 °C

6: acetone / 336 h / 20 °C

With dmap; ammonium hydroxide; lithium aluminium tetrahydride; borane-THF; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;

Reference yield:

: 700-63-0,6485-52-5,6485-67-2,58429-87-1
(R)-phenylglycine amide

: 1609286-15-8
(3R)-1-(chloromethyl)-3-phenyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride

Guidance literature:: Multi-step reaction with 5 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Reflux

2: dmap; triethylamine / dichloromethane / 0 - 20 °C

3: borane-THF / tetrahydrofuran / 0 °C / Reflux

4: N,N-dimethyl-formamide / 12 h / 150 °C

5: acetone / 336 h / 20 °C

With dmap; lithium aluminium tetrahydride; borane-THF; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone;