(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

Base Information

Chemical Name:(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol
CAS No.:900159-10-6
Molecular Formula:C₃₁H₄₂O₃Si
Molecular Weight:490.758
Hs Code.:

Synonyms:(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

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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 (2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

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Technology Process of (2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

There total 5 articles about (2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-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: 99.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 179944-99-1
(2S,4R)-2-Methyl-5-trityloxy-pentane-1,4-diol

: 900159-10-6
(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 2h;
DOI:10.1021/jo0605086

Reference yield:

: 52813-63-5
(5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone

: 900159-10-6
(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 76 percent / pyridine / CH₂Cl₂ / Heating

2.1: n-BuLi; i-Pr₂NH / -15 °C

2.2: 81 percent / -78 °C

3.1: 100 percent / LiAlH₄ / tetrahydrofuran

4.1: 99 percent / imidazole / dimethylformamide / 2 h / 0 °C

With pyridine; 1H-imidazole; lithium aluminium tetrahydride; n-butyllithium; diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0605086

Reference yield:

: 76-83-5
trityl chloride

: 900159-10-6
(2R,4S)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-1-trityloxy-pentan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 76 percent / pyridine / CH₂Cl₂ / Heating

2.1: n-BuLi; i-Pr₂NH / -15 °C

2.2: 81 percent / -78 °C

3.1: 100 percent / LiAlH₄ / tetrahydrofuran

4.1: 99 percent / imidazole / dimethylformamide / 2 h / 0 °C

With pyridine; 1H-imidazole; lithium aluminium tetrahydride; n-butyllithium; diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0605086