[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Base Information

Chemical Name:[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester
CAS No.:255714-99-9
Molecular Formula:C₂₄H₃₂F₃NO₃Si
Molecular Weight:467.604
Hs Code.:

[2-(<i>tert</i>-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Synonyms:[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

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Chemical Property of [2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Chemical Property:

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Technology Process of [2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

There total 4 articles about [2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl 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:

: 109-56-8
i-propyl(2-(hydroxy)ethyl)amine

: 255714-99-9
[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: DMAP / CH₂Cl₂ / 12 h / Heating

2: Et₃N / CH₂Cl₂ / 16 h / 0 - 20 °C

3: tetrahydrofuran / 16 h / Heating

With dmap; triethylamine; In tetrahydrofuran; dichloromethane; 1: Substitution / 2: Acylation / 3: Substitution;
DOI:10.1039/a907174a

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 255714-99-9
[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: DMAP / CH₂Cl₂ / 12 h / Heating

2: Et₃N / CH₂Cl₂ / 16 h / 0 - 20 °C

3: tetrahydrofuran / 16 h / Heating

With dmap; triethylamine; In tetrahydrofuran; dichloromethane; 1: Substitution / 2: Acylation / 3: Substitution;
DOI:10.1039/a907174a

Reference yield:

: 175288-41-2
N-<2-(tert-butyldiphenylsilyloxy)ethyl>-N-isopropylamine

: 255714-99-9
[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid 2,2,2-trifluoro-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 16 h / 0 - 20 °C

2: tetrahydrofuran / 16 h / Heating

With triethylamine; In tetrahydrofuran; dichloromethane; 1: Acylation / 2: Substitution;
DOI:10.1039/a907174a