(10-hydroxyphenanthren-9-yl)(phenyl)methanone

Base Information

• Chemical Name: (10-hydroxyphenanthren-9-yl)(phenyl)methanone
• CAS No.: 28178-98-5
• Molecular Formula: C₂₁H₁₄O₂
• Molecular Weight: 298.341
• Mol file: 28178-98-5.mol

Synonyms:(10-hydroxyphenanthren-9-yl)(phenyl)methanone

Chemical Property of (10-hydroxyphenanthren-9-yl)(phenyl)methanone

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of (10-hydroxyphenanthren-9-yl)(phenyl)methanone

There total 15 articles about (10-hydroxyphenanthren-9-yl)(phenyl)methanone 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: 98.0%

1-([1,1'-biphenyl]-2-yl)-3-phenylprop-2-yn-1-one (1587718-59-9) → (10-hydroxyphenanthren-9-yl)(phenyl)methanone (28178-98-5)

Guidance literature:

With 8-methylquinoline 1-oxide; [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); In fluorobenzene; at 25 ℃; Reagent/catalyst; Solvent; Catalytic behavior;

DOI:10.1002/chem.201600736

Reference yield: 97.0%

9-phenylethynylfluoren-9-ol (117745-96-7) → (10-hydroxyphenanthren-9-yl)(phenyl)methanone (28178-98-5)

Guidance literature:

With 8-methylquinoline 1-oxide; [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); In 1,2-dichloro-ethane; at 20 ℃; for 2h; regioselective reaction; Inert atmosphere;

DOI:10.1021/acs.orglett.5b03160

Reference yield: 94.0%

C21H16O2 → (10-hydroxyphenanthren-9-yl)(phenyl)methanone (28178-98-5)

Guidance literature:

With dichloro(dimethylglyoxime)(dimethylglyoximato)cobalt(III); 9-(2-mesityl)-10-methylacridinium perchlorate; In acetonitrile; at 20 ℃; for 24h; Irradiation; Inert atmosphere;

DOI:10.1021/acs.orglett.0c03665

upstream raw materials:

Benzoic acid 10-benzoyl-phenanthren-9-yl ester

9,10-phenanthrenequinone

2,3-diphenylphenanthro[9,10-b]furan

3-Phenyl-2-p-tolyl-1-oxa-cyclopenta[l]phenanthrene