2-fluoro-6-phenylnaphthalene

Base Information

Chemical Name:2-fluoro-6-phenylnaphthalene
CAS No.:1214368-85-0
Molecular Formula:C₁₆H₁₁F
Molecular Weight:222.262
Hs Code.:

Synonyms:2-fluoro-6-phenylnaphthalene

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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 2-fluoro-6-phenylnaphthalene

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Technology Process of 2-fluoro-6-phenylnaphthalene

There total 2 articles about 2-fluoro-6-phenylnaphthalene 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: 80.0%

: 1132675-28-5
5-fluoro-2-(2-oxo-2-phenylethyl)benzaldehyde

: 536-74-3
phenylacetylene

: 1214368-85-0
2-fluoro-6-phenylnaphthalene

Guidance literature:: With iron(III) chloride; In 1,2-dichloro-ethane; at 60 ℃; Inert atmosphere;
DOI:10.1021/ol4000394

Reference yield:

: 94569-84-3
2-bromo-5-fluorobenzaldehyde

: 98-83-9,6144-04-3,25014-31-7,42612-14-6
isopropenylbenzene

: 1214368-85-0
2-fluoro-6-phenylnaphthalene

Guidance literature:: 2-bromo-5-fluorobenzaldehyde; isopropenylbenzene; With palladium diacetate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; In N,N-dimethyl acetamide; at 135 ℃; for 2h; Inert atmosphere;

With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 80 ℃; for 24h;
DOI:10.1021/jo201339z

Reference yield: 67.0%

: 1214368-85-0
2-fluoro-6-phenylnaphthalene

: 201733-56-4
2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane

: 1268936-08-8
5,5-dimethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborinane

Guidance literature:: With bis(1,5-cyclooctadiene)nickel⁽⁰⁾; sodium phenoxide; tricyclohexylphosphine; In tetrahydrofuran; at 110 ℃; for 15h; Schlenk technique; Inert atmosphere; Glovebox;
DOI:10.1021/jacs.5b08103