1-cyano-amino>-5-hexene

Base Information

Chemical Name:1-cyano-amino>-5-hexene
CAS No.:97998-43-1
Molecular Formula:C₁₈H₂₈N₂Si
Molecular Weight:300.519
Hs Code.:

1-cyano-<N-benzyl-N-<(trimethylsilyl)methyl>amino>-5-hexene

Synonyms:

Suppliers and Price of 1-cyano-amino>-5-hexene

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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 1-cyano-amino>-5-hexene

Chemical Property:

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Technology Process of 1-cyano-amino>-5-hexene

There total 3 articles about 1-cyano-amino>-5-hexene 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:

: 53215-95-5
N-(trimethylsilylmethyl)benzylamine

: 97998-43-1
1-cyano-amino>-5-hexene

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / tetrahydrofuran; H₂O

2: 1.) LDA / 1.) THF, 0 deg C, 30 min, 2.) THF, 25 deg C, 12 h

With lithium diisopropyl amide; In tetrahydrofuran; water;
DOI:10.1021/jo00221a010

Reference yield:

: 100-46-9
benzylamine

: 97998-43-1
1-cyano-amino>-5-hexene

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent / 2.) 0.1 N aq. NaOH / 2.5 h / 200 °C

2: 94 percent / tetrahydrofuran; H₂O

3: 1.) LDA / 1.) THF, 0 deg C, 30 min, 2.) THF, 25 deg C, 12 h

With sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; water;
DOI:10.1021/jo00221a010

Reference yield:

: 87813-07-8
N-benzyl-N-(cyanomethyl)-N-[(trimethylsilyl)methyl]amine

: 1119-51-3
bromopentene

: 97998-43-1
1-cyano-amino>-5-hexene

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, 0 deg C, 30 min, 2.) THF, 25 deg C, 12 h;
DOI:10.1021/jo00221a010