1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one

Base Information

Chemical Name:1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one
CAS No.:79692-10-7
Molecular Formula:C₂₂H₁₈O₂Se
Molecular Weight:393.344
Hs Code.:

Synonyms:

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Chemical Property of 1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one

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Technology Process of 1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one

There total 6 articles about 1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one 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:

: 79692-06-1
methyl 3-(2-benzoylphenyl)-2-chloropropanoate

: 79692-10-7
1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: sodium borohydride / ethanol / 2 h / Ambient temperature

2: sodium borohydride, lithium perchlorate / methanol / 0.5 h / Ambient temperature

3: potassium hydroxide / ethanol; H₂O / 4 h / Heating

4: triethylamine, 2-chloro-1-methylpyridinium iodide / CH₂Cl₂ / 8 h / Heating

With potassium hydroxide; sodium tetrahydroborate; 2-chloro-1-methyl-pyridinium iodide; lithium perchlorate; triethylamine; In methanol; ethanol; dichloromethane; water;

Reference yield:

: 2835-77-0
(2-aminophenyl)(phenyl)methanone

: 79692-10-7
1-phenyl-4-phenylseleno-4,5-dihydro-2-benzoxepin-3(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: 26 percent / cupric chloride, t-butyl nitrite / acetonitrile / 0.17 h / Ambient temperature

2: sodium borohydride / ethanol / 2 h / Ambient temperature

3: sodium borohydride, lithium perchlorate / methanol / 0.5 h / Ambient temperature

4: potassium hydroxide / ethanol; H₂O / 4 h / Heating

5: triethylamine, 2-chloro-1-methylpyridinium iodide / CH₂Cl₂ / 8 h / Heating

With potassium hydroxide; sodium tetrahydroborate; tert.-butylnitrite; 2-chloro-1-methyl-pyridinium iodide; lithium perchlorate; triethylamine; copper dichloride; In methanol; ethanol; dichloromethane; water; acetonitrile;