(1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

Base Information

Chemical Name:(1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one
CAS No.:1382997-51-4
Molecular Formula:C₁₄H₁₄BrNO₄
Molecular Weight:340.173
Hs Code.:

Synonyms:(1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

Suppliers and Price of (1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

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Technology Process of (1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

There total 2 articles about (1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one 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: 77.0%

: 3156-37-4
4-bromo-β-nitrostyrene

: 765-87-7
cyclohexane-1,2-dione

: 1382997-51-4
(1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

Guidance literature:: With nickel diacetate; triethylamine; (1R,2R)-N,N'-di(4'-bromobenzyl)-1,2-diaminocyclohexane; In tetrahydrofuran; at 20 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1039/c2ob25135c

Reference yield:

: 3156-37-4
4-bromo-β-nitrostyrene

: 765-87-7
cyclohexane-1,2-dione

: 1382997-51-4
(1S,5S,6R,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

: (1S,5S,6S,7S)-6-(4-bromophenyl)-1-hydroxy-7-nitrobicyclo[3.2.1]octan-8-one

Guidance literature:: With C₂₄H₂₆N₂O₂; bis(acetylacetonate)nickel(II); In isopropyl alcohol; at 20 ℃; for 3h; Overall yield = 88 %; stereoselective reaction;
DOI:10.1016/j.tetasy.2014.06.011