3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

Base Information

Chemical Name:3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde
CAS No.:158585-04-7
Molecular Formula:C₅₂H₄₈O₆Si
Molecular Weight:797.035
Hs Code.:

Synonyms:3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

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Chemical Property of 3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

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Technology Process of 3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

There total 8 articles about 3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde 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: 75.0%

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

: 158585-04-7
3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

Guidance literature:: With tetrapropylammonium perruthennate; 3 A molecular sieve; 4-methylmorpholine N-oxide; In acetonitrile; at 25 ℃; for 0.5h;

Reference yield:

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

: 158585-04-7
3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

Guidance literature:: Multi-step reaction with 7 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

7: 75 percent / 4-methylmorpholine N-oxide, 3 Angstroem molecular sieves, tetrapropylammonium perruthenate(VII) / acetonitrile / 0.5 h / 25 °C

With 1H-imidazole; n-butyllithium; tetrapropylammonium perruthennate; 3 A molecular sieve; diisobutylaluminium hydride; potassium carbonate; 4-methylmorpholine N-oxide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 158585-04-7
3-Benzyloxy-2-[2,6-bis-benzyloxy-4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzaldehyde

Guidance literature:: Multi-step reaction with 5 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

5: 75 percent / 4-methylmorpholine N-oxide, 3 Angstroem molecular sieves, tetrapropylammonium perruthenate(VII) / acetonitrile / 0.5 h / 25 °C

With 1H-imidazole; n-butyllithium; tetrapropylammonium perruthennate; 3 A molecular sieve; 4-methylmorpholine N-oxide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; acetonitrile;