(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

Base Information

Chemical Name:(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol
CAS No.:182156-18-9
Molecular Formula:C₂₅H₃₈O₆Si
Molecular Weight:462.659
Hs Code.:

Synonyms:(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

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Chemical Property of (R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

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Technology Process of (R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

There total 5 articles about (R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol 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: 98.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 182156-17-8
(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-furan-3-yl-ethane-1,2-diol

: 182156-18-9
(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; for 15h; Ambient temperature;
DOI:10.1021/jo960963+

Reference yield:

: 81028-12-8
(4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-5-carboxaldehyde

: 182156-18-9
(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

Guidance literature:: Multi-step reaction with 5 steps

1: 1) n-BuLi / 1) THF, hexanes, -78 deg C, 30 min, 2) THF, hexanes, -78 deg C, 1.5 h

2: 1) oxalyl chloride, DMSO, 2) Et₃N / 1) CH₂Cl₂, -78 deg C, 30 min, 2) CH₂Cl₂, -78 deg C -> room temperature, 1.5 h

3: 1) n-BuLi / 1) THF, hexanes, 0 deg C -> room temperature, 1 h, 2) THF, hexanes, room temperature, 1 h

4: 1) AD-mix-β, 2) Na2SO3 / 1) t-BuOH, H2O, 0 deg C, 10 h, 2) t-BuOH, H2O, room temperature, 1 h

5: 98 percent / imidazole / dimethylformamide / 15 h / Ambient temperature

With 1H-imidazole; n-butyllithium; oxalyl dichloride; AD-mix-β; dimethyl sulfoxide; triethylamine; sodium sulfite; In N,N-dimethyl-formamide;
DOI:10.1021/jo960963+

Reference yield:

: ((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-furan-3-yl-methanol

: 182156-18-9
(R)-1-((4R,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(tert-butyl-dimethyl-silanyloxy)-1-furan-3-yl-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: 1) oxalyl chloride, DMSO, 2) Et₃N / 1) CH₂Cl₂, -78 deg C, 30 min, 2) CH₂Cl₂, -78 deg C -> room temperature, 1.5 h

2: 1) n-BuLi / 1) THF, hexanes, 0 deg C -> room temperature, 1 h, 2) THF, hexanes, room temperature, 1 h

3: 1) AD-mix-β, 2) Na2SO3 / 1) t-BuOH, H2O, 0 deg C, 10 h, 2) t-BuOH, H2O, room temperature, 1 h

4: 98 percent / imidazole / dimethylformamide / 15 h / Ambient temperature

With 1H-imidazole; n-butyllithium; oxalyl dichloride; AD-mix-β; dimethyl sulfoxide; triethylamine; sodium sulfite; In N,N-dimethyl-formamide;
DOI:10.1021/jo960963+