((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

Base Information

Chemical Name:((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate
CAS No.:956005-85-9
Molecular Formula:C₂₁H₂₆N₂O₄
Molecular Weight:370.448
Hs Code.:

Synonyms:((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

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Chemical Property of ((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

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Technology Process of ((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

There total 7 articles about ((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate 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: 95.0%

: (R)-3-amino-4-phenylmethyl-2-oxazolidinone

: 956006-31-8
C₁₁H₁₆O₃

: 956005-85-9
((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃;
DOI:10.1021/ol7017938

Reference yield:

: 956006-23-8
((1S,6R)-6-((1,3-dithian-2-yl)methyl)cyclohex-3-enyl)-methanol

: 956005-85-9
((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 20 °C

2: 53 percent / MeI / acetonitrile; H₂O / 24 h

3: 95 percent / TsOH*H₂O / CH₂Cl₂ / 20 °C

With dmap; toluene-4-sulfonic acid; triethylamine; methyl iodide; In dichloromethane; water; acetonitrile;
DOI:10.1021/ol7017938

Reference yield:

: 956005-64-4
((1S,6S)-6-((tert-butyldimethylsilyloxy)methyl)cyclohex-3-enyl)methyl iodide

: 956005-85-9
((1S,6R)-6-((E)-2-((R)-4-benzyl-2-oxooxazolidin-3-ylimino)ethyl)cyclohex-3-enyl)methyl acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: HMPA; n-BuLi / tetrahydrofuran; hexane / 1 h / -78 °C

1.2: tetrahydrofuran; hexane / 12 h / -78 - 20 °C

1.3: 32 percent / Bu₄NF / tetrahydrofuran / 3 h

2.1: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 20 °C

3.1: 53 percent / MeI / acetonitrile; H₂O / 24 h

4.1: 95 percent / TsOH*H₂O / CH₂Cl₂ / 20 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; n-butyllithium; toluene-4-sulfonic acid; triethylamine; methyl iodide; In tetrahydrofuran; hexane; dichloromethane; water; acetonitrile;
DOI:10.1021/ol7017938