1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

Base Information

Chemical Name:1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene
CAS No.:163770-91-0
Molecular Formula:C₃₈H₃₁NO₅
Molecular Weight:581.668
Hs Code.:

Synonyms:1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

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Chemical Property of 1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

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Technology Process of 1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

There total 4 articles about 1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene 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: 82.0%

: 163770-80-7
1-Hydroxy-3-<(4-cyanobenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

: 163770-91-0
1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

Guidance literature:: With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; potassium iodide; In water; 1,2-dichloro-ethane; for 18h; Heating;
DOI:10.1021/jo00110a038

Reference yield:

: 874-60-2
4-methyl-benzoyl chloride

: 163770-91-0
1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / AlCl₃ / CH₂Cl₂ / 72 h / Ambient temperature

2: 63 percent / K₂CO₃, KI, Bu₄NHSO₄ / 1,2-dichloro-ethane; H₂O / 18 h / Heating

3: 82 percent / K₂CO₃, KI, Bu₄NHSO₄ / 1,2-dichloro-ethane; H₂O / 18 h / Heating

With aluminium trichloride; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; potassium iodide; In dichloromethane; water; 1,2-dichloro-ethane;
DOI:10.1021/jo00110a038

Reference yield:

: 163770-78-3
1,3-Dihydroxy-4,6-di(4-methylbenzoyl)benzene

: 163770-91-0
1-<(4-Cyanobenzyl)oxy>-3-<(4-methoxybenzyl)oxy>-4,6-bis(4-methylbenzoyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃, KI, Bu₄NHSO₄ / 1,2-dichloro-ethane; H₂O / 18 h / Heating

2: 82 percent / K₂CO₃, KI, Bu₄NHSO₄ / 1,2-dichloro-ethane; H₂O / 18 h / Heating

With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; potassium iodide; In water; 1,2-dichloro-ethane;
DOI:10.1021/jo00110a038