(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

Base Information

Chemical Name:(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide
CAS No.:1620165-47-0
Molecular Formula:C₂₅H₃₉NOSi
Molecular Weight:397.676
Hs Code.:

Synonyms:(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

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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 (Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

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Technology Process of (Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

There total 3 articles about (Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide 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: 97.0%

: 1620165-24-3
C₁₄H₁₉NO

: 181934-30-5
1-[(triisopropylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one

: 1620165-47-0
(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

Guidance literature:: With tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate; Trimethylacetic acid; In acetone; at 20 ℃; for 12h;
DOI:10.1039/c4cc04072d

Reference yield:

: 35863-45-7
2,2-dimethyl-3-phenylpropanenitrile

: 1620165-47-0
(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: diethyl ether / 2 h / 0 °C / Inert atmosphere

1.2: 2 h / 0 - 20 °C / Inert atmosphere

2.1: tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate; Trimethylacetic acid / acetone / 12 h / 20 °C

With tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate; Trimethylacetic acid; In diethyl ether; acetone;
DOI:10.1039/c4cc04072d

Reference yield:

: 100-39-0
benzyl bromide

: 1620165-47-0
(Z)-N-(2,2-dimethyl-1-phenyl-6-(triisopropylsilyl)hex-3-en-5-yn-3-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C

1.2: 20 °C

2.1: diethyl ether / 2 h / 0 °C / Inert atmosphere

2.2: 2 h / 0 - 20 °C / Inert atmosphere

3.1: tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate; Trimethylacetic acid / acetone / 12 h / 20 °C

With tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hexafluoroantimonate; lithium diisopropyl amide; Trimethylacetic acid; In tetrahydrofuran; diethyl ether; acetone;
DOI:10.1039/c4cc04072d