(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

Base Information

Chemical Name:(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde
CAS No.:1054634-48-8
Molecular Formula:C₂₂H₃₆O₆Si
Molecular Weight:424.61
Hs Code.:

Synonyms:(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

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Chemical Property of (R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

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Technology Process of (R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

There total 4 articles about (R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde 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:

: 844473-73-0
(2S)-2-[(4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-2-(methoxymethoxy)ethanol

: 1054634-48-8
(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; at -78 - 0 ℃;
DOI:10.1021/jo0483116

Reference yield:

: 677300-65-1
(4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-4-[(1S)-2-(tert-butyldimethylsilyloxy)-1-benzoyloxyethyl]-2,2-dimethyl-6-phenyl-[1,3]dioxane

: 1054634-48-8
(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / K₂CO₃ / methanol / 24 h / 20 °C

2: 85 percent / DIPEA / CH₂Cl₂ / 12 h / Heating

3: 94 percent / HF*pyridine; pyridine / tetrahydrofuran / 12 h / 20 °C

4: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 0 °C

With pyridine; oxalyl dichloride; potassium carbonate; pyridine hydrogenfluoride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; 4: Swern oxidation;
DOI:10.1021/jo0483116

Reference yield:

: 844473-71-8
(1S)-2-(tert-butyldimethylsilyloxy)-1-[(4R,5R,6R)-5-(tert-butyldimethylsilyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]ethanol

: 1054634-48-8
(R)-[(4R,5R,6R)-5-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-phenyl-[1,3]dioxan-4-yl]-methoxymethoxy-acetaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / DIPEA / CH₂Cl₂ / 12 h / Heating

2: 94 percent / HF*pyridine; pyridine / tetrahydrofuran / 12 h / 20 °C

3: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 0 °C

With pyridine; oxalyl dichloride; pyridine hydrogenfluoride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 3: Swern oxidation;
DOI:10.1021/jo0483116