3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

Base Information

Chemical Name:3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol
CAS No.:871702-81-7
Molecular Formula:C₃₈H₅₁NO₇Si
Molecular Weight:661.911
Hs Code.:

3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

Synonyms:3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

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Chemical Property of 3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

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Technology Process of 3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

There total 5 articles about 3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-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:

: 871702-78-2
benzyl({(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl)amine

: 871702-81-7
3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / H₂ / Pd(OH)2/C / ethanol / 20 °C

2: 1.29 g / LiNTf₂ / CH₂Cl₂ / 12 h / 20 °C

3: 967 mg / Na₂CO₃*H₂O / dioxane; H₂O / 20 °C

With hydrogen; sodium carbonate; bis(trifluoromethane)sulfonimide lithium; palladium dihydroxide; In 1,4-dioxane; ethanol; dichloromethane; water;
DOI:10.1002/ejoc.200500386

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 871702-81-7
3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 72 percent / imidazole / CH₂Cl₂ / 2.5 h / 0 - 20 °C

2: 88 percent / H₂ / Pd(OH)2/C / ethanol / 20 °C

3: 1.29 g / LiNTf₂ / CH₂Cl₂ / 12 h / 20 °C

4: 967 mg / Na₂CO₃*H₂O / dioxane; H₂O / 20 °C

With 1H-imidazole; hydrogen; sodium carbonate; bis(trifluoromethane)sulfonimide lithium; palladium dihydroxide; In 1,4-dioxane; ethanol; dichloromethane; water;
DOI:10.1002/ejoc.200500386

Reference yield:

: 603959-03-1
(4R,5S)-[5-(benzylaminomethyl)-2,2-dimethyl[1,3]dioxolan-4-yl]methanol

: 871702-81-7
3-benzyloxy-1-({[(4S,5R)-5-[(tert-butyldimethylsilyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl](fluoren-9-ylmethoxycarbonyl)amino)propan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 72 percent / imidazole / CH₂Cl₂ / 2.5 h / 0 - 20 °C

2: 88 percent / H₂ / Pd(OH)2/C / ethanol / 20 °C

3: 1.29 g / LiNTf₂ / CH₂Cl₂ / 12 h / 20 °C

4: 967 mg / Na₂CO₃*H₂O / dioxane; H₂O / 20 °C

With 1H-imidazole; hydrogen; sodium carbonate; bis(trifluoromethane)sulfonimide lithium; palladium dihydroxide; In 1,4-dioxane; ethanol; dichloromethane; water;
DOI:10.1002/ejoc.200500386