4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester

Base Information

• Chemical Name: 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester
• CAS No.: 478012-70-3
• Molecular Formula: C₃₄H₃₇BrO₆
• Molecular Weight: 621.568
• Mol file: 478012-70-3.mol

Synonyms:4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester

Chemical Property of 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester

There total 14 articles about 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-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: 83.0%

4-allyl-5-methyl-4-(3-methyl-but-2-enyl)-cyclohexane-1,3-dione (478012-58-7) + 4-bromo-benzoic acid 2-cyanocarbonyl-3-(2-methyl-allyloxy)-benzyl ester (478012-54-3) → 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester (478012-70-3)

Guidance literature:

With dmap; triethylamine; In tetrahydrofuran; at 25 ℃;

DOI:10.1021/ja0509984

Reference yield:

(2,2-dimethyl-4H-benzo[d][1,3]dioxin-5-yl)methanol (112429-70-6) → 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester (478012-70-3)

Guidance literature:

Multi-step reaction with 7 steps

1: 97 percent / 4-(dimethylamino)pyridine; Et₃N / CH₂Cl₂ / 0.33 h / 25 °C

2: 85 percent / aq. p-TsOH / tetrahydrofuran / 10 h / 75 °C

3: 87 percent / MnO₂ / ethyl acetate / 1.5 h / 25 °C

4: 91 percent / K₂CO₃ / acetone / 2 h / 56 °C

5: 82 percent / toluene / 0 - 25 °C

6: 73 percent / pyridinium chlorochromate / CH₂Cl₂ / 12 h / 40 °C

7: 83 percent / Et₃N; 4-(dimethylamino)pyridine / tetrahydrofuran / 25 °C

With dmap; manganese(IV) oxide; potassium carbonate; toluene-4-sulfonic acid; triethylamine; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane; ethyl acetate; acetone; toluene;

DOI:10.1021/ja0509984

Reference yield:

4-bromo-benzoic acid 2-formyl-3-hydroxy-benzyl ester (478012-53-2) → 4-bromo-benzoic acid 2-[3-allyl-4-methyl-3-(3-methyl-but-2-enyl)-2,6-dioxo-cyclohexanecarbonyl]-3-(2-methyl-allyloxy)-benzyl ester (478012-70-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 91 percent / K₂CO₃ / acetone / 2 h / 56 °C

2: 82 percent / toluene / 0 - 25 °C

3: 73 percent / pyridinium chlorochromate / CH₂Cl₂ / 12 h / 40 °C

4: 83 percent / Et₃N; 4-(dimethylamino)pyridine / tetrahydrofuran / 25 °C

With dmap; potassium carbonate; triethylamine; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane; acetone; toluene;

DOI:10.1021/ja0509984

upstream raw materials:

4-allyl-5-methyl-4-(3-methyl-but-2-enyl)-cyclohexane-1,3-dione

4-bromo-benzoic acid 2-cyanocarbonyl-3-(2-methyl-allyloxy)-benzyl ester

4-chlorobenzoyl chloride

(2,2-dimethyl-4H-benzo[d][1,3]dioxin-5-yl)methanol