2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester

Base Information

• Chemical Name: 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester
• CAS No.: 167832-44-2
• Molecular Formula: C₃₇H₃₃BrO₆
• Molecular Weight: 653.569
• Mol file: 167832-44-2.mol

Synonyms:2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester

Chemical Property of 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester

There total 3 articles about 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl 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: 51.0%

(1-bromo-2-naphthyl)methanol (76635-70-6) + 3,5-Bis-benzyloxy-4-chlorocarbonyl-benzoic acid tert-butyl ester (158980-58-6) → 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester (167832-44-2)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 20 ℃;

DOI:10.1021/jm020018f

Reference yield:

1-bromo-2-naphthoic acid (20717-79-7) → 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester (167832-44-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 89 percent / BH₃ / tetrahydrofuran / 5 h / 20 °C

2: 51 percent / DMAP; Et₃N / CH₂Cl₂ / 20 °C

With dmap; borane; triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jm020018f

Reference yield:

2,6-bis(benzyloxy)-4-<(1,1-dimethylethoxy)carbonyl>benzoic acid (158980-56-4) → 2,6-dibenzyloxy-4-(1,1-dimethylethoxycarbonyl)benzoic acid 2-(1-bromonaphthyl)methyl ester (167832-44-2)

Guidance literature:

Multi-step reaction with 2 steps

1: oxalyl chloride / CH₂Cl₂; dimethylformamide / 3 h / 20 °C

2: 51 percent / DMAP; Et₃N / CH₂Cl₂ / 20 °C

With dmap; oxalyl dichloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm020018f

upstream raw materials:

(1-bromo-2-naphthyl)methanol

3,5-Bis-benzyloxy-4-chlorocarbonyl-benzoic acid tert-butyl ester

1-bromo-2-naphthoic acid

2,6-bis(benzyloxy)-4-<(1,1-dimethylethoxy)carbonyl>benzoic acid

Downstream raw materials:

3,5-dibenzyloxy-4-(2-benzyloxycarbonyl-1-naphthylcarbonyl)benzoic acid 1,1-dimethylethyl ester

3,5-dibenzyloxy-4-(2-benzyloxycarbonyl-1-naphthylcarbonyl)benzoic acid

1-(2,6-bis-benzyloxy-4-tert-butoxycarbonyl-benzoyl)-naphthalene-2-carboxylic acid

3,5-dibenzyloxy-4-(2-formyl-1-naphthylcarbonyl)benzoic acid 1,1-dimethylethyl ester