(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

Base Information

Chemical Name:(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine
CAS No.:1260510-37-9
Molecular Formula:C₂₉H₃₈N₂O₂Si
Molecular Weight:474.718
Hs Code.:

Synonyms:(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

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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 (3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

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Technology Process of (3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

There total 6 articles about (3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine 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: 86.0%

: 1260396-21-1
(R)-1-[1-(tert-butyldiphenylsiloxy)pentan-3-yl]-4-(4-methoxyphenyl)-1H-tetrazol-5-(4H)-thione

: 1260510-37-9
(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

Guidance literature:: With hydrogenchloride; hydrogen; In water; at 20 ℃; for 120h; under 4560.31 Torr;
DOI:10.1021/ol102892f

Reference yield:

: 1260396-07-3
(3R)-3-[4-(4-methoxyphenyl)-5-thioxo-1H-tetrazol-1-yl]pentan-1-ol

: 1260510-37-9
(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole; dmap / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

2: hydrogenchloride; hydrogen / water / 120 h / 20 °C / 4560.31 Torr

With 1H-imidazole; hydrogenchloride; dmap; hydrogen; In tetrahydrofuran; water;
DOI:10.1021/ol102892f

Reference yield:

: 13980-76-2
1-(4-methoxyphenyl)-1H-tetrazole-5-thiol

: 1260510-37-9
(3R,E)-N-(1-(tertbutyldiphenylsilyloxy)pentan-3-yl)-N'-(4-methoxyphenyl)formamidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: (S)-2-{bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilanyl)oxy]methyl}pyrrolidine; benzoic acid / toluene / 0.5 h / -30 °C

1.2: 92 h / -30 °C

2.1: sodium tetrahydroborate / methanol; toluene / 1.5 h / -78 - -30 °C

3.1: 1H-imidazole; dmap / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

4.1: hydrogenchloride; hydrogen / water / 120 h / 20 °C / 4560.31 Torr

With 1H-imidazole; (S)-2-{bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilanyl)oxy]methyl}pyrrolidine; hydrogenchloride; dmap; sodium tetrahydroborate; hydrogen; benzoic acid; In tetrahydrofuran; methanol; water; toluene; 1.1: aza-Michael reaction / 1.2: aza-Michael reaction;
DOI:10.1021/ol102892f