N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine

Base Information

• Chemical Name: N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine
• CAS No.: 86724-46-1
• Molecular Formula: C₁₅H₂₄N₂Si
• Molecular Weight: 260.454
• Mol file: 86724-46-1.mol

Synonyms:N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine

Chemical Property of N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine

There total 4 articles about N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine 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:

Methyl N-methylanthranilate (85-91-6) → N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine (86724-46-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 92.7 percent / diethyl ether / addition at 0 deg C then reflux (0.5 h)

2: 78.1 percent / 250 °C

3: 96.1 percent / 96 h / Heating

4: 1) methyl trifluoromethanesulfonate, 2) Et₃N / 1) CH₂Cl₂, 25 deg C, 4 h, 2) -20 deg C, 0.5 h

With triethylamine; methyl trifluoromethanesulfonate; In diethyl ether;

DOI:10.1016/S0040-4020(01)96709-2

Reference yield:

N-methyl-2-(1-methylethenyl)benzenamine (7117-17-1) → N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine (86724-46-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 96.1 percent / 96 h / Heating

2: 1) methyl trifluoromethanesulfonate, 2) Et₃N / 1) CH₂Cl₂, 25 deg C, 4 h, 2) -20 deg C, 0.5 h

With triethylamine; methyl trifluoromethanesulfonate;

DOI:10.1016/S0040-4020(01)96709-2

Reference yield:

2-(2-methylamino)phenyl-2-propanol (67759-79-9) → N-(2-Isopropenyl-phenyl)-N-methyl-N'-trimethylsilanylmethyl-formamidine (86724-46-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 78.1 percent / 250 °C

2: 96.1 percent / 96 h / Heating

3: 1) methyl trifluoromethanesulfonate, 2) Et₃N / 1) CH₂Cl₂, 25 deg C, 4 h, 2) -20 deg C, 0.5 h

With triethylamine; methyl trifluoromethanesulfonate;

DOI:10.1016/S0040-4020(01)96709-2

upstream raw materials:

N-trimethylsilylmethylamine

N-(2-Isopropenyl-phenyl)-N-methyl-formamide

N-methyl-2-(1-methylethenyl)benzenamine

2-(2-methylamino)phenyl-2-propanol

Downstream raw materials:

1-benzoyl-3a,8-dimethyl-1,2,3,3a,8,8a-hexahydro-pyrrolo[2,3-b]indole

(+/-)-1-benzoyl-3a,8-dimethyl-(3ar,8ac)-1,2,3,3a,8,8a-hexahydro-pyrrolo[2,3-b]indole