C₃₀H₃₈N₄O₁₀

Base Information

Chemical Name:C₃₀H₃₈N₄O₁₀
CAS No.:166271-29-0
Molecular Formula:C₃₀H₃₈N₄O₁₀
Molecular Weight:614.653
Hs Code.:

C<sub>30</sub>H<sub>38</sub>N<sub>4</sub>O<sub>10</sub>

Synonyms:

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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 C₃₀H₃₈N₄O₁₀

Chemical Property:

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Technology Process of C₃₀H₃₈N₄O₁₀

There total 7 articles about C₃₀H₃₈N₄O₁₀ 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:

: 1792-81-0
cis-1,2-cyclohexane

: 166271-29-0
C₃₀H₃₈N₄O₁₀

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) NaH / 1.) THF, room temp., 1 h, 2.) room temp., 40 h

2: 1.) NaH / 1.) THF, room temp., 1 h, 2.) THF, reflux, 18 h

3: 61 percent / TsOH, H₂ / Pd/C / dioxane / Ambient temperature

4: 47 percent / NaH, KBF₄ / tetrahydrofuran / 96 h / Heating

5: 80 percent / LiAlH₄ / tetrahydrofuran / 15 h / Heating

6: 90 percent / CAN / acetonitrile / 1.5 h / Ambient temperature

7: 81 percent / conc. H₂SO₄ / ethanol / 1.5 h / Ambient temperature

With lithium aluminium tetrahydride; ammonium cerium(IV) nitrate; sulfuric acid; hydrogen; sodium hydride; toluene-4-sulfonic acid; potassium tetrafluoroborate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol; acetonitrile;

Reference yield:

: 125992-58-7
(1S,2R)-2-(benzyloxy)cyclohexan-1-ol

: 166271-29-0
C₃₀H₃₈N₄O₁₀

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) THF, room temp., 1 h, 2.) THF, reflux, 18 h

2: 61 percent / TsOH, H₂ / Pd/C / dioxane / Ambient temperature

3: 47 percent / NaH, KBF₄ / tetrahydrofuran / 96 h / Heating

4: 80 percent / LiAlH₄ / tetrahydrofuran / 15 h / Heating

5: 90 percent / CAN / acetonitrile / 1.5 h / Ambient temperature

6: 81 percent / conc. H₂SO₄ / ethanol / 1.5 h / Ambient temperature

With lithium aluminium tetrahydride; ammonium cerium(IV) nitrate; sulfuric acid; hydrogen; sodium hydride; toluene-4-sulfonic acid; potassium tetrafluoroborate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol; acetonitrile;

Reference yield:

: 51329-29-4,51329-30-7,85761-38-2,85761-39-3,116661-88-2,116661-89-3,125992-58-7
(+/-)-cis-2-(benzyloxy)cyclohexanol

: 166271-29-0
C₃₀H₃₈N₄O₁₀

Guidance literature:: Multi-step reaction with 7 steps

1: diisopropyl ether / 50 h / Ambient temperature; lipase YS

2: 1.) NaH / 1.) THF, room temp., 1 h, 2.) THF, reflux, 18 h

3: 61 percent / TsOH, H₂ / Pd/C / dioxane / Ambient temperature

4: 47 percent / NaH, KBF₄ / tetrahydrofuran / 96 h / Heating

5: 80 percent / LiAlH₄ / tetrahydrofuran / 15 h / Heating

6: 90 percent / CAN / acetonitrile / 1.5 h / Ambient temperature

7: 81 percent / conc. H₂SO₄ / ethanol / 1.5 h / Ambient temperature

With lithium aluminium tetrahydride; ammonium cerium(IV) nitrate; sulfuric acid; hydrogen; sodium hydride; toluene-4-sulfonic acid; potassium tetrafluoroborate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol; di-isopropyl ether; acetonitrile;