[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester
CAS No.:187099-52-1
Molecular Formula:C₂₁H₃₁NO₂Si
Molecular Weight:357.568
Hs Code.:

Synonyms:[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

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Chemical Property of [2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of [2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

There total 6 articles about [2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester 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: 86.0%

: 870-63-3
prenyl bromide

: 187099-49-6
2-((trimethylsilyl)ethynyl)phenylaminocarboxylic acid tert-butyl ester

: 187099-52-1
[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: 2-((trimethylsilyl)ethynyl)phenylaminocarboxylic acid tert-butyl ester; With tert.-butyl lithium; In diethyl ether; at -20 ℃;

prenyl bromide; In diethyl ether; at -78 - 20 ℃; for 5h;
DOI:10.7164/antibiotics.54.105

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 187099-52-1
[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 86 percent / iPr₂NEt / tetrahydrofuran / 120 h / 80 °C

2.1: 88 percent / CuI; Et₃N / Pd(PPh₃)2Cl₂ / 0.67 h / 20 °C

3.1: tBuLi / diethyl ether / -20 °C

3.2: 86 percent / diethyl ether / 5 h / -78 - 20 °C

With copper(l) iodide; tert.-butyl lithium; triethylamine; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; diethyl ether;
DOI:10.7164/antibiotics.54.105

Reference yield:

: 615-43-0
2-iodophenylamine

: 187099-52-1
[2-(3-Methyl-but-2-enyl)-6-trimethylsilanylethynyl-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 86 percent / iPr₂NEt / tetrahydrofuran / 120 h / 80 °C

2.1: 88 percent / CuI; Et₃N / Pd(PPh₃)2Cl₂ / 0.67 h / 20 °C

3.1: tBuLi / diethyl ether / -20 °C

3.2: 86 percent / diethyl ether / 5 h / -78 - 20 °C

With copper(l) iodide; tert.-butyl lithium; triethylamine; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; diethyl ether;
DOI:10.7164/antibiotics.54.105