1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Base Information

Chemical Name:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate
CAS No.:1453115-00-8
Molecular Formula:BF₄*C₂₆H₃₄N₃O
Molecular Weight:491.38
Hs Code.:

Synonyms:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Suppliers and Price of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

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 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

There total 9 articles about 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate 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:

: C₂₆H₃₄N₃O⁽¹⁺⁾*Br^(1-)

: 1453115-00-8
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Guidance literature:: With sodium tetrafluoroborate; In acetone; at 20 ℃;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 31795-93-4
N-benzyl-L-proline

: 1453115-00-8
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

2.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

3.1: hydrazine / ethanol / 2 h / Reflux

3.2: 0.5 h / Heating

4.1: methanol / 20 °C

5.1: acetic acid / ethanol / 24 h / 20 °C

6.1: chloroform / 72 h / 20 °C / Reflux

7.1: sodium tetrafluoroborate / acetone / 20 °C

With lithium aluminium tetrahydride; sodium tetrafluoroborate; acetic acid; triphenylphosphine; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; chloroform; acetone;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

: 1453115-00-8
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-3-butoxy-4-methyl-5-phenyl-1H-imidazolium tetrafluoroborate

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium hydroxide / isopropyl alcohol

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

3.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

4.1: hydrazine / ethanol / 2 h / Reflux

4.2: 0.5 h / Heating

5.1: methanol / 20 °C

6.1: acetic acid / ethanol / 24 h / 20 °C

7.1: chloroform / 72 h / 20 °C / Reflux

8.1: sodium tetrafluoroborate / acetone / 20 °C

With lithium aluminium tetrahydride; sodium tetrafluoroborate; acetic acid; triphenylphosphine; potassium hydroxide; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; chloroform; isopropyl alcohol; acetone;
DOI:10.1016/j.tetasy.2013.07.013