2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

Base Information

Chemical Name:2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide
CAS No.:898269-36-8
Molecular Formula:C₂₆H₅₁NO₂Si
Molecular Weight:437.782
Hs Code.:

Synonyms:2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

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Chemical Property of 2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

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Technology Process of 2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

There total 1 articles about 2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide 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: 30.0%

: Triethyl-[(1R,3aR,4S,7aR)-1-((R)-3-iodo-1-methyl-propyl)-7a-methyl-octahydro-inden-4-yloxy]-silane

: 6830-83-7
N-methyl-pivalamide

: 898269-36-8
2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

Guidance literature:: With sodium hydride; In tetrahydrofuran; for 20h; Heating;
DOI:10.1016/j.bmc.2006.05.050

Reference yield:

: 898269-36-8
2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

: N-((R)-3-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Dihydroxy-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-butyl)-2,2,N-trimethyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

2.1: 9.0 mg / pyridinium dichromate / CH₂Cl₂ / 12 h / 20 °C

3.1: n-BuLi / tetrahydrofuran; hexane / -78 °C

3.2: 31 percent / tetrahydrofuran; hexane / -78 °C

4.1: 4.0 mg / tetrabutylammonium fluoride / tetrahydrofuran / -78 - 20 °C

With dipyridinium dichromate; n-butyllithium; tetrabutyl ammonium fluoride; In tetrahydrofuran; hexane; dichloromethane; 3.2: Horner-Wadsworth-Emmons reaction;
DOI:10.1016/j.bmc.2006.05.050

Reference yield:

: 898269-36-8
2,2,N-Trimethyl-N-[(R)-3-((1R,3aR,4S,7aR)-7a-methyl-4-triethylsilanyloxy-octahydro-inden-1-yl)-butyl]-propionamide

: 898269-98-2
N-((R)-3-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-butyl)-2,2,N-trimethyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

2.1: 9.0 mg / pyridinium dichromate / CH₂Cl₂ / 12 h / 20 °C

3.1: n-BuLi / tetrahydrofuran; hexane / -78 °C

3.2: 31 percent / tetrahydrofuran; hexane / -78 °C

With dipyridinium dichromate; n-butyllithium; tetrabutyl ammonium fluoride; In tetrahydrofuran; hexane; dichloromethane; 3.2: Horner-Wadsworth-Emmons reaction;
DOI:10.1016/j.bmc.2006.05.050