(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

Base Information

Chemical Name:(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane
CAS No.:193970-24-0
Molecular Formula:C₂₈H₅₀O₄Si₂
Molecular Weight:506.874
Hs Code.:

Synonyms:(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

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Chemical Property of (2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

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Technology Process of (2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

There total 5 articles about (2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane 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:

: 193970-21-7
[(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-phenyl-[1,3]dioxan-4-yl]-acetaldehyde

: 4-{1-[(tert-butyldimethylsilyl)oxy]butyl}(triphenyl)phosphonium iodide

: 193970-24-0
(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

Guidance literature:: With lithium hexamethyldisilazane; Yield given. Multistep reaction; 1) THF, toluene, 0 deg C, 2) THF, toluene, 8 h;
DOI:10.1021/ja971219p

Reference yield:

: 22900-10-3,35536-75-5,36792-85-5,113890-34-9,113890-37-2,133813-23-7
2-deoxy-D-ribose

: 193970-24-0
(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

Guidance literature:: Multi-step reaction with 5 steps

1: dimethylformamide / 15 h / 25 °C

2: dimethylformamide / 15 h / 25 °C

3: 90 percent / imidazole / CH₂Cl₂ / 12 h / 25 °C

4: 1.) O₃, 2.) Ph₃P / 1.) CH₂Cl₂, -78 deg C, 10 min, 2.) CH₂Cl₂, 25 deg C, 3 h

5: 1.) LiHMDS / 1.) toluene, THF, 0 deg C, 20 min, 2.) toluene, THF, 0 deg C, 1 h; 25 deg C, 7 h

With 1H-imidazole; ozone; triphenylphosphine; lithium hexamethyldisilazane; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 78606-78-7
methyl (E,5S,6R)-5,6,7-trihydroxyhept-2-enoate

: 193970-24-0
(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-4-[(Z)-6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-2-phenyl-[1,3]dioxane

Guidance literature:: Multi-step reaction with 4 steps

1: dimethylformamide / 15 h / 25 °C

2: 90 percent / imidazole / CH₂Cl₂ / 12 h / 25 °C

3: 1.) O₃, 2.) Ph₃P / 1.) CH₂Cl₂, -78 deg C, 10 min, 2.) CH₂Cl₂, 25 deg C, 3 h

4: 1.) LiHMDS / 1.) toluene, THF, 0 deg C, 20 min, 2.) toluene, THF, 0 deg C, 1 h; 25 deg C, 7 h

With 1H-imidazole; ozone; triphenylphosphine; lithium hexamethyldisilazane; In dichloromethane; N,N-dimethyl-formamide;