(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

Base Information

Chemical Name:(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol
CAS No.:1380424-12-3
Molecular Formula:C₃₄H₂₉F₃N₂O₄
Molecular Weight:586.61
Hs Code.:

Synonyms:(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

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Chemical Property of (S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

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Technology Process of (S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

There total 4 articles about (S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol 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%

: 1380423-95-9
(S)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yne-1,2-diol

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 1380424-12-3
(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

Guidance literature:: With pyridine; In pyridine; for 5h; Inert atmosphere; Cooling with ice;

Reference yield:

: 1380423-98-2
(S)-3-(4-(4-(tert-butyldimethylsilyloxy)-5-(tert-butyldiphenylsilyloxy )pent-1-ynyl)phenyl)-3-(trifluoromethyl)diaziridine

: 1380424-12-3
(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; iodine / methanol / 0.5 h / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

3: pyridine / pyridine / 5 h / Inert atmosphere; Cooling with ice

With pyridine; tetrabutyl ammonium fluoride; iodine; triethylamine; In tetrahydrofuran; pyridine; methanol;

Reference yield:

: 1380423-99-3
(S)-3-(4-(4-(tert-butyldimethylsilyloxy)-5-(tert-butyldiphenylsilyloxy )pent-1-ynyl)phenyl)-3-(trifluoromethyl)-3H-diazirine

: 1380424-12-3
(S)-1-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenyl)pent-4-yn-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

2: pyridine / pyridine / 5 h / Inert atmosphere; Cooling with ice

With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; pyridine;