[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester
CAS No.:927823-83-4
Molecular Formula:C₄₄H₆₀N₂O₅Si₂
Molecular Weight:753.142
Hs Code.:

[4-(<i>tert</i>-butyl-diphenyl-silanyloxy)-1-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid <i>tert</i>-butyl ester

Synonyms:[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

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Chemical Property of [4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

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Technology Process of [4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

There total 7 articles about [4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-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:

: 927823-82-3
4-azido-5-(tert-butyl-diphenyl-silanyloxy)-2-(tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-pentanoic acid amide

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

: 927823-83-4
[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium; In ethanol; at 20 ℃; under 760 Torr;
DOI:10.1021/ja0670409

Reference yield:

: 927824-64-4
4-chloro-2,4-dicyano-2-methyl-thiobutyric acid S-methyl ester

: 927823-83-4
[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: NaN₃ / dimethylsulfoxide / 42 h / 20 °C

2: TMSCl / 48 h / 0 °C

3: NaBH₄ / Hg(OAc)2 / ethanol / 0.5 h / 0 °C

4: imidazole / dimethylformamide / 12 h / 20 °C

5: PtH(PMe₂OH)(PMe₂O)2H / ethanol / 12 h / 80 °C

6: H₂ / Pd / ethanol / 20 °C / 760 Torr

With 1H-imidazole; sodium tetrahydroborate; chloro-trimethyl-silane; sodium azide; hydrogen; (Me₂PO)2HPt(Me₂POH); mercury(II) diacetate; palladium; In ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/ja0670409

Reference yield:

: 927823-80-1
4-azido-5-hydroxy-2-hydroxymethyl-2-methyl-pentanenitrile

: 927823-83-4
[4-(tert-butyl-diphenyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-carbamoyl-3-methyl-butyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: imidazole / dimethylformamide / 12 h / 20 °C

2: PtH(PMe₂OH)(PMe₂O)2H / ethanol / 12 h / 80 °C

3: H₂ / Pd / ethanol / 20 °C / 760 Torr

With 1H-imidazole; hydrogen; (Me₂PO)2HPt(Me₂POH); palladium; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/ja0670409