2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

Base Information

Chemical Name:2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile
CAS No.:312327-02-9
Molecular Formula:C₂₂H₃₀N₂O₃Si
Molecular Weight:398.577
Hs Code.:

Synonyms:2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

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Chemical Property of 2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

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Technology Process of 2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

There total 3 articles about 2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile 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%

: 312327-01-8
2-(tert-butyldimethylsilyloxy)-2-(4-benzyloxy-3-methoxy-5-nitrophenyl)ethanonitrile

: 312327-02-9
2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

Guidance literature:: With hydrogenchloride; titanium(III) chloride; ammonium acetate; In acetone; at 20 ℃; for 12h;
DOI:10.1021/jo001080s

Reference yield:

: 6635-20-7
isonitrovanillin

: 312327-02-9
2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: 92 percent / KOH; benzyltriethylammonium chloride / CH₂Cl₂ / 24 h / 20 °C

2.1: 18-crown-6; ZnI₂ / acetonitrile / 0.25 h / 20 °C

2.2: 92 percent / acetonitrile / 3 h / 70 °C

3.1: 86 percent / aq. NH₄O₂CCH₃; TiCl₃; aq. HCl / acetone / 12 h / 20 °C

With hydrogenchloride; potassium hydroxide; titanium(III) chloride; 18-crown-6 ether; ammonium acetate; N-benzyl-N,N,N-triethylammonium chloride; zinc(II) iodide; In dichloromethane; acetone; acetonitrile; 1.1: Alkylation / 2.1: Addition / 2.2: silylation / 3.1: Reduction;
DOI:10.1021/jo001080s

Reference yield:

: 100-39-0
benzyl bromide

: 312327-02-9
2-(5-amino-4-benzyloxy-3-methoxyphenyl)-2-(tert-butyldimethylsilyloxy)ethanonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: 92 percent / KOH; benzyltriethylammonium chloride / CH₂Cl₂ / 24 h / 20 °C

2.1: 18-crown-6; ZnI₂ / acetonitrile / 0.25 h / 20 °C

2.2: 92 percent / acetonitrile / 3 h / 70 °C

3.1: 86 percent / aq. NH₄O₂CCH₃; TiCl₃; aq. HCl / acetone / 12 h / 20 °C

With hydrogenchloride; potassium hydroxide; titanium(III) chloride; 18-crown-6 ether; ammonium acetate; N-benzyl-N,N,N-triethylammonium chloride; zinc(II) iodide; In dichloromethane; acetone; acetonitrile; 1.1: Alkylation / 2.1: Addition / 2.2: silylation / 3.1: Reduction;
DOI:10.1021/jo001080s