1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

Base Information

Chemical Name:1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene
CAS No.:183559-15-1
Molecular Formula:C₄₈H₅₈O₄Si₂
Molecular Weight:755.157
Hs Code.:

Synonyms:1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

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Chemical Property of 1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

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Technology Process of 1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

There total 3 articles about 1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene 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: 63.0%

: 183559-14-0
1-[(5R,7S)-8-Bromo-5,7-bis-(tert-butyl-diphenyl-silanyloxy)-oct-2-ynyloxymethyl]-4-methoxy-benzene

: 183559-15-1
1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide; In tetrahydrofuran; at 0 ℃; for 2h;
DOI:10.1016/0040-4039(96)01700-5

Reference yield:

: 183559-12-8
(R)-6-(4-Methoxy-benzyloxy)-1-(S)-oxiranyl-hex-4-yn-2-ol

: 183559-15-1
1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / Li₂NiBr₄ / tetrahydrofuran / 2.5 h / Ambient temperature

2: 80 percent / imidazole, DMAP / CH₂Cl₂; diethyl ether / 12 h

3: 63 percent / 0.1 M SmI₂, HMPA / tetrahydrofuran / 2 h / 0 °C

With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; samarium diiodide; dilithium tetrabromonickelate(II); In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/0040-4039(96)01700-5

Reference yield:

: 183559-13-9
(2S,4R)-1-Bromo-8-(4-methoxy-benzyloxy)-oct-6-yne-2,4-diol

: 183559-15-1
1-{2-[(3R,5R)-3,5-Bis-(tert-butyl-diphenyl-silanyloxy)-cyclohexylidene]-ethoxymethyl}-4-methoxy-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / imidazole, DMAP / CH₂Cl₂; diethyl ether / 12 h

2: 63 percent / 0.1 M SmI₂, HMPA / tetrahydrofuran / 2 h / 0 °C

With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; samarium diiodide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1016/0040-4039(96)01700-5