2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol

Base Information

• Chemical Name: 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol
• CAS No.: 852810-67-4
• Molecular Formula: C₂₁H₃₀O₄Si
• Molecular Weight: 374.552
• Mol file: 852810-67-4.mol

Synonyms:2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol

Chemical Property of 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol

There total 3 articles about 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol 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:

methyl 4-(benzyloxy)-3-hydroxy-5-methoxybenzoate (852810-63-0) → 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol (852810-67-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 91 percent / LiAlH₄ / tetrahydrofuran

2: 71 percent / imidazole / CH₂Cl₂

With 1H-imidazole; lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane;

DOI:10.1016/j.tetlet.2005.03.046

Reference yield:

methyl 3,4-dihydroxy-5-methoxybenzoate (3934-86-9) → 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol (852810-67-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 70 percent / K₂CO₃ / dimethylformamide

2: 91 percent / LiAlH₄ / tetrahydrofuran

3: 71 percent / imidazole / CH₂Cl₂

With 1H-imidazole; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2005.03.046

Reference yield:

benzyl bromide (100-39-0) → 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenol (852810-67-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 70 percent / K₂CO₃ / dimethylformamide

2: 91 percent / LiAlH₄ / tetrahydrofuran

3: 71 percent / imidazole / CH₂Cl₂

With 1H-imidazole; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2005.03.046

upstream raw materials:

methyl 4-(benzyloxy)-3-hydroxy-5-methoxybenzoate

methyl 3,4-dihydroxy-5-methoxybenzoate

benzyl bromide

Downstream raw materials:

2-benzyloxy-6-iodo-4-methoxy-benzoic acid 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenyl ester

2-iodo-4,6-dimethoxy-benzoic acid 2-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-phenyl ester

10-benzyloxy-11-hydroxy-2,4,9-trimethoxy-7H-dibenzo[c,e]oxepin-5-one

4-benzyloxy-1-hydroxymethyl-3,7,9-trimethoxy-benzo[c]chromen-6-one