trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

Base Information

Chemical Name:trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester
CAS No.:791838-48-7
Molecular Formula:C₁₉H₁₇F₃O₄S
Molecular Weight:398.403
Hs Code.:

Synonyms:trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

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Chemical Property of trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

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Technology Process of trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

There total 8 articles about trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl 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:

: 7484-37-9
(3-phenylpropyl)triphenylphosphonium bromide

: 791838-48-7
trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / n-BuLi / tetrahydrofuran / 0 - 25 °C

2: 99 percent / H₂ / Pd/C / ethyl acetate

3: 96 percent / LiAlH₄ / tetrahydrofuran / 20 °C

4: 90 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂

5: MCPBA / CHCl₃

6: HCl / methanol

7: pyridine / 0 - 25 °C

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; hydrogen; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethyl acetate; 1: Wittig olefination / 4: Swern oxidation / 5: Baeyer-Villiger oxidation;
DOI:10.1016/j.bmcl.2004.07.055

Reference yield:

: 532399-76-1
ethyl 2-Formylbenzo[b]furan-4-carboxylate

: 791838-48-7
trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / n-BuLi / tetrahydrofuran / 0 - 25 °C

2: 99 percent / H₂ / Pd/C / ethyl acetate

3: 96 percent / LiAlH₄ / tetrahydrofuran / 20 °C

4: 90 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂

5: MCPBA / CHCl₃

6: HCl / methanol

7: pyridine / 0 - 25 °C

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; hydrogen; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethyl acetate; 1: Wittig olefination / 4: Swern oxidation / 5: Baeyer-Villiger oxidation;
DOI:10.1016/j.bmcl.2004.07.055

Reference yield:

: 532399-77-2
2-((E)-4-Phenyl-but-1-enyl)-benzofuran-4-carboxylic acid ethyl ester

: 791838-48-7
trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / H₂ / Pd/C / ethyl acetate

2: 96 percent / LiAlH₄ / tetrahydrofuran / 20 °C

3: 90 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂

4: MCPBA / CHCl₃

5: HCl / methanol

6: pyridine / 0 - 25 °C

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; oxalyl dichloride; hydrogen; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethyl acetate; 3: Swern oxidation / 4: Baeyer-Villiger oxidation;
DOI:10.1016/j.bmcl.2004.07.055