(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

Base Information

Chemical Name:(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal
CAS No.:500220-30-4
Molecular Formula:C₂₀H₃₄O₄Si
Molecular Weight:366.573
Hs Code.:

Synonyms:(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

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Chemical Property of (2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

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Technology Process of (2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

There total 9 articles about (2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal 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: 96.0%

: 500220-31-5
(2S,3R)-N-methoxy-N-methyl-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentamide

: 500220-30-4
(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

Guidance literature:: With di(tert-butyl)aluminium hydride; In tetrahydrofuran; hexane; at -50 ℃; for 0.5h;
DOI:10.1021/ja061938g

Reference yield:

: 866530-02-1
(2S,3R)-N-methoxy-N-methyl-3-hydroxy-5-(4-methoxybenzyloxy)-2-methylpentamide

: 500220-30-4
(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

Guidance literature:: Multi-step reaction with 2 steps

1: imidazole; DMAP / dimethylformamide / 20 h / 20 °C

2: 96 percent / tBu₂AlH / tetrahydrofuran; hexane / 0.5 h / -50 °C

With 1H-imidazole; dmap; di(tert-butyl)aluminium hydride; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/ja061938g

Reference yield:

: 900171-30-4
(3S,4R)-4-[2-(4-methoxybenzyloxy)ethyl]-3-methyloxetan-2-one

: 500220-30-4
(2S,3R)-3-(tert-butyldimethylsilanyloxy)-5-(4-methoxybenzyloxy)-2-methylpentanal

Guidance literature:: Multi-step reaction with 3 steps

1: dimethylaluminum chloride / CH₂Cl₂; hexane / 2 h / -25 °C

2: imidazole; DMAP / dimethylformamide / 20 h / 20 °C

3: 96 percent / tBu₂AlH / tetrahydrofuran; hexane / 0.5 h / -50 °C

With 1H-imidazole; dmap; dimethylaluminum chloride; di(tert-butyl)aluminium hydride; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja061938g