[Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile

Base Information

• Chemical Name: [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile
• CAS No.: 96617-25-3
• Molecular Formula: C₁₆H₂₀N₂O
• Molecular Weight: 256.348
• Mol file: 96617-25-3.mol

Synonyms:[Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile

Chemical Property of [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile

There total 2 articles about [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile 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: 65.0%

isopropenyllithium (6386-71-6) + [Benzyl-(2-oxo-cyclobutyl)-amino]-acetonitrile (96617-35-5) → [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile (96617-25-3)

Guidance literature:

In tetrahydrofuran; at -78 ℃;

DOI:10.1021/jo00213a049

Reference yield:

benzylaminoacetonitrile (3010-05-7) → [Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile (96617-25-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 75 percent / methanol / 25 °C

2: 65 percent / tetrahydrofuran / -78 °C

In tetrahydrofuran; methanol;

DOI:10.1021/jo00213a049

Reference yield: 88.0%

[Benzyl-((1R,2R)-2-hydroxy-2-isopropenyl-cyclobutyl)-amino]-acetonitrile (96617-25-3) → (3aS,6aS)-1-Benzyl-3a-methyl-hexahydro-cyclopenta[b]pyrrol-4-one (96617-31-1)

Guidance literature:

With silver nitrate; In ethanol; at 50 ℃; for 15h;

DOI:10.1021/jo00213a049

upstream raw materials:

isopropenyllithium

[Benzyl-(2-oxo-cyclobutyl)-amino]-acetonitrile

benzylaminoacetonitrile

Downstream raw materials:

(3aS,6aS)-1-Benzyl-3a-methyl-hexahydro-cyclopenta[b]pyrrol-4-one