9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

Base Information

Chemical Name:9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene
CAS No.:905440-71-3
Molecular Formula:C₁₉H₁₅F₆N
Molecular Weight:371.325
Hs Code.:

Synonyms:9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

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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 9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

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Technology Process of 9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

There total 3 articles about 9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene 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: 85.0%

: 905440-70-2
9-benzyl-2,3-bis-trifluoromethyl-1,4-dihydro-1,4-epiazano-naphthalene

: 905440-71-3
9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 9h;
DOI:10.1021/ja0658259

Reference yield:

: 25473-60-3
2-benzyl-2H-isoindole

: 905440-71-3
9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 3.5 h / -20 °C

2: 85 percent / H₂ / Pd/C / methanol / 9 h / 20 °C

With hydrogen; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1021/ja0658259

Reference yield:

: 2142-01-0
N-benzylphthalimide

: 905440-71-3
9-benzyl-2,3-bis-trifluoromethyl-1,2,3,4-tetrahydro-1,4-epiazano-naphthalene

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / LiAlH₄; methanol / tetrahydrofuran / 0.5 h / -78 °C

2: CH₂Cl₂ / 3.5 h / -20 °C

3: 85 percent / H₂ / Pd/C / methanol / 9 h / 20 °C

With methanol; lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja0658259