(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

Base Information

Chemical Name:(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone
CAS No.:171564-62-8
Molecular Formula:C₅₂H₅₀O₆Si
Molecular Weight:799.051
Hs Code.:

Synonyms:(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

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Chemical Property of (2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

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Technology Process of (2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

There total 7 articles about (2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone 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: 86.0%

: 158585-03-6
2,6-Bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoic acid 3-benzyloxy-2-bromo-benzyl ester

: 171564-62-8
(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

Reference yield:

: 16534-12-6
3,5-dihydroxy-4-bromobenzoic acid

: 171564-62-8
(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

Guidance literature:: Multi-step reaction with 6 steps

1: 96 percent / K₂CO₃ / dimethylformamide / 4 h / 25 °C

2: 100 percent / DIBALH / CH₂Cl₂; toluene / 1 h / 0 °C

3: 82 percent / imidazole / dimethylformamide / 1 h / 25 °C

4: 60 percent / n-BuLi / tetrahydrofuran; hexane / 1.) -78 deg C, 30 min, 2.) -78 to 25 deg C, 30 min

5: 93 percent / Ph₃P, DEAD / tetrahydrofuran / 0.67 h / 25 °C

6: 86 percent / n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

With 1H-imidazole; n-butyllithium; diisobutylaluminium hydride; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 171564-62-8
(2-Benzyloxy-6-hydroxymethyl-phenyl)-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / imidazole / dimethylformamide / 1 h / 25 °C

2: 60 percent / n-BuLi / tetrahydrofuran; hexane / 1.) -78 deg C, 30 min, 2.) -78 to 25 deg C, 30 min

3: 93 percent / Ph₃P, DEAD / tetrahydrofuran / 0.67 h / 25 °C

4: 86 percent / n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

With 1H-imidazole; n-butyllithium; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;