3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

Base Information

Chemical Name:3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester
CAS No.:171564-69-5
Molecular Formula:C₄₅H₄₂O₅Si
Molecular Weight:690.911
Hs Code.:

Synonyms:3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

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Chemical Property of 3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

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Technology Process of 3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

There total 8 articles about 3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester 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: 98.0%

: 100-39-0
benzyl bromide

: 171564-68-4
3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid

: 171564-69-5
3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 25 ℃; for 2h;

Reference yield:

: 6908-41-4,58590-49-1
4-(methoxycarbonyl)benzyl alcohol

: 171564-69-5
3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 100 percent / imidazole / dimethylformamide / 2 h / 25 °C

2: 62 percent / LiOH / dioxane; H₂O / 24 h / 25 °C

3: 96 percent / Ph₃P, DEAD / tetrahydrofuran / 0.25 h / 25 °C

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

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

6: 94 percent / 2-methyl-2-butene, aq. NaH₂PO₄, 80percent NaClO₂ / tetrahydrofuran; 2-methyl-propan-2-ol / 8 h / 25 °C

7: 98 percent / K₂CO₃ / dimethylformamide / 2 h / 25 °C

With 1H-imidazole; lithium hydroxide; sodium chlorite; sodium dihydrogenphosphate; n-butyllithium; tetrapropylammonium perruthennate; 2-methyl-but-2-ene; 3 A molecular sieve; potassium carbonate; 4-methylmorpholine N-oxide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; hexane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;

Reference yield:

: 113068-93-2
4-(tert-Butyl-diphenyl-silanyloxymethyl)-benzoic acid

: 171564-69-5
3-Benzyloxy-2-[4-(tert-butyl-diphenyl-silanyloxymethyl)-benzoyl]-benzoic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 96 percent / Ph₃P, DEAD / tetrahydrofuran / 0.25 h / 25 °C

2: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C

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

4: 94 percent / 2-methyl-2-butene, aq. NaH₂PO₄, 80percent NaClO₂ / tetrahydrofuran; 2-methyl-propan-2-ol / 8 h / 25 °C

5: 98 percent / K₂CO₃ / dimethylformamide / 2 h / 25 °C

With sodium chlorite; sodium dihydrogenphosphate; n-butyllithium; tetrapropylammonium perruthennate; 2-methyl-but-2-ene; 3 A molecular sieve; potassium carbonate; 4-methylmorpholine N-oxide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;