Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Base Information

Chemical Name:Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate
CAS No.:130050-89-4
Molecular Formula:C₂₄H₃₄O₅Si
Molecular Weight:430.616
Hs Code.:

Synonyms:Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Suppliers and Price of Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

There total 3 articles about Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate 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:

: 102732-44-5
ethyl (S)-2-(tert-butyldiphenylsilyloxy)propanoate

: 130050-89-4
Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / diisobutylaluminum hydride / diethyl ether / 1.5 h / -100 °C

2: 1) LDA / 1) THF, -70 deg C, 30 min

With diisobutylaluminium hydride; lithium diisopropyl amide; In diethyl ether;
DOI:10.1016/0008-6215(90)84068-6

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 130050-89-4
Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / imidazole / dimethylformamide / Ambient temperature

2: 91 percent / diisobutylaluminum hydride / diethyl ether / 1.5 h / -100 °C

3: 1) LDA / 1) THF, -70 deg C, 30 min

With 1H-imidazole; diisobutylaluminium hydride; lithium diisopropyl amide; In diethyl ether; N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(90)84068-6

Reference yield:

: 17639-76-8,92935-45-0
methyl 2-methoxypropionate

: 87696-33-1
(S)-2-(O-tert-butyldiphenylsilyloxy)propanal

: 130192-75-5
(3R,4S,5S)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-3,5-dimethyl-dihydro-furan-2-one

: 130050-89-4
Methyl (2S,3S,4S)-3-hydroxy-2-methyl-2-methoxy-4-<(1,1-dimethylethyldiphenylsilyl)oxy>pentanoate

: 130050-90-7
(2R,3S,4S)-4-(tert-Butyl-diphenyl-silanyloxy)-3-hydroxy-2-methoxy-2-methyl-pentanoic acid methyl ester

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction. Yields of byproduct given; 1) THF, -70 deg C, 30 min;
DOI:10.1016/0008-6215(90)84068-6