(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

Base Information

Chemical Name:(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine
CAS No.:1450733-35-3
Molecular Formula:C₁₇H₃₁NO₃Si
Molecular Weight:325.524
Hs Code.:

Synonyms:(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

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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 (S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

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Technology Process of (S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

There total 6 articles about (S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine 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: 100.0%

: 1450733-34-2
(S)-(1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethyl)carbamic acid benzyl ester

: 1450733-35-3
(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 3h;
DOI:10.1016/j.bmc.2013.06.018

Reference yield:

: 1450733-33-1
(S)-(1-(4-hydroxybenzyl)-2,2-dimethoxyethyl)carbamic acid benzyl ester

: 1450733-35-3
(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

2: 5%-palladium/activated carbon; hydrogen / methanol / 3 h / 20 °C

With 1H-imidazole; 5%-palladium/activated carbon; hydrogen; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.06.018

Reference yield:

: 13512-31-7
N-(benzyloxycarbonyl)-L-tyrosine methyl ester

: 1450733-35-3
(S)-1-(4-(tert-butyldimethylsilyloxy)benzyl)-2,2-dimethoxyethan-1-amine

Guidance literature:: Multi-step reaction with 5 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

2: diisobutylaluminium hydride / dichloromethane / 2.67 h / -78 °C / Inert atmosphere

3: toluene-4-sulfonic acid / 12 h / 20 °C / Inert atmosphere

4: 1H-imidazole / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

5: 5%-palladium/activated carbon; hydrogen / methanol / 3 h / 20 °C

With 1H-imidazole; 5%-palladium/activated carbon; hydrogen; diisobutylaluminium hydride; toluene-4-sulfonic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.06.018