methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

Base Information

Chemical Name:methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester
CAS No.:455330-55-9
Molecular Formula:C₂₉H₄₃NO₆SSi
Molecular Weight:561.815
Hs Code.:

methanesulfonic acid 4-<i>tert</i>-butoxycarbonylamino-3-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

Synonyms:methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

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Chemical Property of methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

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Technology Process of methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

There total 8 articles about methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl 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: 98.0%

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

: 455330-45-7
Methanesulfonic acid (1R,3R,4R)-4-azido-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

: 455330-55-9
methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol;

Reference yield:

: 96894-00-7
(1S,2S)-4,4-ethylenedioxy-2-hydroxymethylcyclohexanol

: 455330-55-9
methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 84 percent / imidazole; DMAP / dimethylformamide

2: 100 percent / aq. acetic acid / dimethylformamide

3: 92 percent / DMAP / pyridine

4: 86 percent / sodium borohydride / methanol

5: 95 percent / sodium azide / dimethylformamide

6: 90 percent / DMAP / pyridine

7: 98 percent / hydrogen / Pd/C / methanol

With 1H-imidazole; dmap; sodium tetrahydroborate; sodium azide; hydrogen; acetic acid; palladium on activated charcoal; In pyridine; methanol; N,N-dimethyl-formamide;

Reference yield:

: 96893-99-1
(1R,2S)-5,5-(Ethylendioxy)-2-hydroxycyclohexancarbonsaeure-ethylester

: 455330-55-9
methanesulfonic acid 4-tert-butoxycarbonylamino-3-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohexyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 98 percent / DMAP / pyridine

2: 99 percent / lithium aluminum hydride / diethyl ether

3: 84 percent / imidazole; DMAP / dimethylformamide

4: 100 percent / aq. acetic acid / dimethylformamide

5: 92 percent / DMAP / pyridine

6: 86 percent / sodium borohydride / methanol

7: 95 percent / sodium azide / dimethylformamide

8: 90 percent / DMAP / pyridine

9: 98 percent / hydrogen / Pd/C / methanol

With 1H-imidazole; dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium azide; hydrogen; acetic acid; palladium on activated charcoal; In pyridine; methanol; diethyl ether; N,N-dimethyl-formamide;