(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

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Chemical Name:(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile
CAS No.:130814-78-7
Molecular Formula:C₁₉H₁₆N₄O
Molecular Weight:316.362
Hs Code.:

Synonyms:(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

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Chemical Property of (S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

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Technology Process of (S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

There total 3 articles about (S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile 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%

: 130814-75-4
(-)-{1-(R)-[(1E)-2-methylbuta-1,3-dienyloxy]ethyl}benzene

: 670-54-2
ethenetetracarbonitrile

: 130814-78-7
(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

Guidance literature:: In tetrahydrofuran; at -30 ℃;
DOI:10.1055/s-1990-26986

Reference yield:

: 1517-69-7
(R)-1-phenylethanol

: 130814-78-7
(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / p-TsOH / 1 Torr

2: 1) LDA / 1) THF, hexane, -60 deg C, 2) -60 deg C -> rt, 1 h

3: 95 percent / tetrahydrofuran / -30 °C

With toluene-4-sulfonic acid; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1055/s-1990-26986

Reference yield:

: 130814-73-2
(E)-(1'R)-2-Methyl-3-(1'-phenylethoxy)-propenal

: 130814-78-7
(S)-4-Methyl-3-((R)-1-phenyl-ethoxy)-cyclohex-4-ene-1,1,2,2-tetracarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 1) LDA / 1) THF, hexane, -60 deg C, 2) -60 deg C -> rt, 1 h

2: 95 percent / tetrahydrofuran / -30 °C

With lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1055/s-1990-26986