2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid

Base Information

• Chemical Name: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid
• CAS No.: 220658-28-6
• Molecular Formula: C₂₃H₂₄O₆
• Molecular Weight: 396.44

Synonyms:2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid

Chemical Property of 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid

Chemical Property:

Purity/Quality:

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Technology Process of 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid

There total 4 articles about 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid 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:

2-Iodophenol (533-58-4) → 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid (220658-28-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 82 percent / K₂CO₃ / acetone / 6 h / Heating

2: 85 percent / Na₂CO₃ / (Ph₃P)4Pd / dimethylformamide / 3 h / 90 °C

3: 1.) MeI, 2.) NaOH / 1.) DMF, 70 deg C, 1 d, 2.) DMF, water, 100 deg C, 12 h

With sodium hydroxide; sodium carbonate; potassium carbonate; methyl iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In N,N-dimethyl-formamide; acetone;

DOI:10.3987/COM-98-8342

Reference yield:

tert-butyl 4-bromobutyrate (110661-91-1) → 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid (220658-28-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 82 percent / K₂CO₃ / acetone / 6 h / Heating

2: 85 percent / Na₂CO₃ / (Ph₃P)4Pd / dimethylformamide / 3 h / 90 °C

3: 1.) MeI, 2.) NaOH / 1.) DMF, 70 deg C, 1 d, 2.) DMF, water, 100 deg C, 12 h

With sodium hydroxide; sodium carbonate; potassium carbonate; methyl iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In N,N-dimethyl-formamide; acetone;

DOI:10.3987/COM-98-8342

Reference yield:

t-butyl 4-(2-iodophenyloxy)butyrate (220658-25-3) → 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxylic acid (220658-28-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / Na₂CO₃ / (Ph₃P)4Pd / dimethylformamide / 3 h / 90 °C

2: 1.) MeI, 2.) NaOH / 1.) DMF, 70 deg C, 1 d, 2.) DMF, water, 100 deg C, 12 h

With sodium hydroxide; sodium carbonate; methyl iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In N,N-dimethyl-formamide;

DOI:10.3987/COM-98-8342

upstream raw materials:

5-(4,4-dimethyl-2-oxazolin-2-yl)-2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran

2-Iodophenol

tert-butyl 4-bromobutyrate

t-butyl 4-(2-iodophenyloxy)butyrate

Downstream raw materials:

N-diphenylmethyl-2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-5-carboxamide

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