(R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal

Base Information

• Chemical Name: (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal
• CAS No.: 1424192-30-2
• Molecular Formula: C₁₉H₃₂O₃Si
• Molecular Weight: 336.547
• Mol file: 1424192-30-2.mol

Synonyms:(R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal

Chemical Property of (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal

There total 3 articles about (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal 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:

tert-butyldimethylsilyl chloride (18162-48-6) → (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal (1424192-30-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 1H-imidazole / N,N-dimethyl-formamide / 5 h / 20 °C / Inert atmosphere

2: dichloromethane / 2 h / -78 - -40 °C / Inert atmosphere

With 1H-imidazole; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1002/cjoc.201200695

Reference yield:

(((2R,3R)-3-(2-(benzyloxy)ethyl)-3-methyloxiran-2-yl)methoxy)(tert-butyl)dimethylsilane (1424192-27-7) + methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide) (118495-99-1) → (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal (1424192-30-2)

Guidance literature:

In dichloromethane; at -78 - -40 ℃; for 2h; Inert atmosphere;

DOI:10.1002/cjoc.201200695

Reference yield:

4-bromo-2,6-di-tert-butylphenol (1139-52-2) → (R)-4-(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-2-methylbutanal (1424192-30-2)

Guidance literature:

Multi-step reaction with 2 steps

1: dichloromethane / 0 °C / Inert atmosphere

2: dichloromethane / 2 h / -78 - -40 °C / Inert atmosphere

In dichloromethane;

DOI:10.1002/cjoc.201200695

upstream raw materials:

(((2R,3R)-3-(2-(benzyloxy)ethyl)-3-methyloxiran-2-yl)methoxy)(tert-butyl)dimethylsilane

methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide)

tert-butyldimethylsilyl chloride

4-bromo-2,6-di-tert-butylphenol

Downstream raw materials:

(S)-(2-(2-(benzyloxy)ethyl)-2-methylbut-3-enyloxy)(tert-butyl)dimethylsilane

(S)-2-(2-(benzyloxy)ethyl)-2-methylbut-3-en-1-ol

(2S)-2-[(2-(benzyloxy)ethyl)]-2-methylbut-3-enyl 2-diazoacetate

(1S,5S,6R)-5-(2-(benzyloxy)ethyl)-5-methyl-3-oxabicyclo[4.1.0]heptan-2-one