1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

Base Information

Chemical Name:1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole
CAS No.:194417-17-9
Molecular Formula:C₃₉H₂₉N₇
Molecular Weight:595.706
Hs Code.:

Synonyms:1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

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Chemical Property of 1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

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Technology Process of 1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

There total 8 articles about 1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole 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: 58.0%

: 95-14-7,27556-51-0
1,2,3-Benzotriazole

: 124750-51-2
N-(triephenylmethyl)-5-<4'-(bromomethyl)-biphenyl-2-yl>tetrazole

: 194417-17-9
1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; 1.) 1h, 2.) 0 deg C, 4 h; r.t., overnight;

Reference yield:

: 611-20-1
salicylonitrile

: 194417-17-9
1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / pyridine / 1.) 0 deg C, 5 min, 2.) r.t., 25 h

2: 1.) Mg, I₂; n-Bu₃SnCl, 2.) Pd(PPh₃)2Cl₂, LiCl / 1.) THF, reflux, 30 min; THF, reflux, 20 h, 2.) DMF, 98 deg C, 24 h

3: 1.) NaN₃, n-Bu₃SnCl, 2.) NaOH / 1.) toluene, 115 deg C, 70 h, 2.) toluene, r.t., 3 h

4: NBS, AIBN / CCl₄ / 3 h / Heating

5: 58 percent / NaH / dimethylformamide / 0 °C / 1.) 1h, 2.) 0 deg C, 4 h; r.t., overnight

With pyridine; bis-triphenylphosphine-palladium(II) chloride; sodium hydroxide; N-Bromosuccinimide; sodium azide; 2,2'-azobis(isobutyronitrile); tributyltin chloride; iodine; sodium hydride; magnesium; lithium chloride; In tetrachloromethane; N,N-dimethyl-formamide;

Reference yield:

: 624-31-7
4-tolyl iodide

: 194417-17-9
1-[2'-(1-triphenylmethyl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-benzotriazole

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) Mg, I₂; n-Bu₃SnCl, 2.) Pd(PPh₃)2Cl₂, LiCl / 1.) THF, reflux, 30 min; THF, reflux, 20 h, 2.) DMF, 98 deg C, 24 h

2: 1.) NaN₃, n-Bu₃SnCl, 2.) NaOH / 1.) toluene, 115 deg C, 70 h, 2.) toluene, r.t., 3 h

3: NBS, AIBN / CCl₄ / 3 h / Heating

4: 58 percent / NaH / dimethylformamide / 0 °C / 1.) 1h, 2.) 0 deg C, 4 h; r.t., overnight

With bis-triphenylphosphine-palladium(II) chloride; sodium hydroxide; N-Bromosuccinimide; sodium azide; 2,2'-azobis(isobutyronitrile); tributyltin chloride; iodine; sodium hydride; magnesium; lithium chloride; In tetrachloromethane; N,N-dimethyl-formamide;