1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

Base Information

Chemical Name:1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone
CAS No.:140160-13-0
Molecular Formula:2C₆H₈O*C₃₆H₂₄Cl₂O₂
Molecular Weight:751.749
Hs Code.:

1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

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Chemical Property of 1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

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Technology Process of 1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

There total 3 articles about 1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone 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: 91.0%

: 930-68-7
cyclohexenone

: 140137-58-2,141987-23-7
(-)-1,4-Bis<3-(o-chlorophenyl)-3-hydroxy-3-phenylprop-1-ynyl>benzene

: 140160-13-0
1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

Guidance literature:: In diethyl ether; hexane; for 6h; Ambient temperature;

Reference yield:

: 106-37-6
1.4-dibromobenzene

: 140160-13-0
1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: 80.2 percent / NEt₃, CuI, PPh₃ / PdCl₂(PPh₃)2 / 4 h / Heating

2: 91 percent / diethyl ether; hexane / 6 h / Ambient temperature

With copper(l) iodide; triethylamine; triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; In diethyl ether; hexane;

Reference yield:

: 13732-87-1
(-)-1-phenyl-1-(o-chlorophenyl)-2-propyn-1-ol

: 140160-13-0
1-(2-Chloro-phenyl)-3-{4-[3-(2-chloro-phenyl)-3-hydroxy-3-phenyl-prop-1-ynyl]-phenyl}-1-phenyl-prop-2-yn-1-ol; compound with cyclohex-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: 80.2 percent / NEt₃, CuI, PPh₃ / PdCl₂(PPh₃)2 / 4 h / Heating

2: 91 percent / diethyl ether; hexane / 6 h / Ambient temperature

With copper(l) iodide; triethylamine; triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; In diethyl ether; hexane;