endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobutnaphthalene-8b-carbonitrile

• Chemical Name: endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobutnaphthalene-8b-carbonitrile
• Molecular Formula: C₁₉H₁₇NO
• Molecular Weight: 275.35
• Mol file: 76514-27-7.mol

Synonyms:

Chemical Property of endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobut

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobut

There total 1 articles about endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobutnaphthalene-8b-carbonitrile 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:

vinyl phenyl ether (766-94-9) + 1-Cyanonaphthalene (86-53-3) → endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobutnaphthalene-8b-carbonitrile (76514-27-7)

Guidance literature:

With hydrogen; palladium on activated charcoal; Yield given. Multistep reaction; 1.) irradiated, 2.) CH₃OH;

Reference yield:

endo-1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobutnaphthalene-8b-carbonitrile (76514-27-7) → vinyl phenyl ether (766-94-9) + Δ-3,4-naphthalene-1-carbonitrile (73599-59-4)

Guidance literature:

With terephthalonitrile; phenanthrene; In acetonitrile; Product distribution; Quantum yield; Mechanism; Irradiation; other cyclobutanaphthalenes, various reaction conditions;

upstream raw materials:

vinyl phenyl ether

1-Cyanonaphthalene

Downstream raw materials:

vinyl phenyl ether

Δ-3,4-naphthalene-1-carbonitrile