N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

Base Information

Chemical Name:N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide
CAS No.:1346763-13-0
Molecular Formula:C₁₇H₂₆ClNO₃Si
Molecular Weight:355.937
Hs Code.:

Synonyms:N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

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Chemical Property of N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

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Technology Process of N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

There total 5 articles about N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide 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: 94.0%

: 1254102-36-7
4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyaniline

: 814-68-6,25189-84-8
acryloyl chloride

: 1346763-13-0
N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

Guidance literature:: With N,N-diethyl-N-isopropylamine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 35019-78-4
ethyl 4-amino-5-chloro-2-methoxybenzoate

: 1346763-13-0
N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / Reflux

2: 1H-imidazole / N,N-dimethyl-formamide / 0 - 20 °C

3: N,N-diethyl-N-isopropylamine / dichloromethane / 2 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; N,N-diethyl-N-isopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 7206-70-4
4-amino-5-chloro-2-methoxybenzoic acid

: 1346763-13-0
N-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-chloro-5-methoxyphenyl]acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / 6 h / 65 °C / High pressure

2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / Reflux

3: 1H-imidazole / N,N-dimethyl-formamide / 0 - 20 °C

4: N,N-diethyl-N-isopropylamine / dichloromethane / 2 h / 20 °C

With 1H-imidazole; hydrogenchloride; lithium aluminium tetrahydride; N,N-diethyl-N-isopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;