(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

Base Information

Chemical Name:(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester
CAS No.:1027565-89-4
Molecular Formula:C₄₀H₃₁NO₆
Molecular Weight:621.689
Hs Code.:

Synonyms:(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

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Chemical Property of (S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

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Technology Process of (S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

There total 8 articles about (S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid 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:

: methyl (R)-4-(1,3-dioxoisoindolin-2-yl)-2-hydroxybutanoate

: 250279-11-9
4'-(2-benzyl-benzofuran-3-yl)-biphenyl-4-ol

: 1027565-89-4
(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In benzene; at 20 ℃; for 0.5h;
DOI:10.1021/jm990560c

Reference yield:

: 36372-16-4
1-(4-bromophenyl)-2-phenoxyethan-1-one

: 1027565-89-4
(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 74 percent / polyphosphoric acid / xylene / 12 h / Heating

2.1: 77 percent / Na₂CO₃; Pd(PPh₃)4 / toluene / 12 h / Heating

3.1: 87 percent / BBr₃ / CH₂Cl₂ / 10 h / 20 °C

4.1: n-BuLi / tetrahydrofuran / 3 h / -40 °C

4.2: 71 percent / tetrahydrofuran / 0.5 h / 0 °C

5.1: hydrazine monohydrate; diethylene glycol / 1 h / 180 °C

5.2: 94 percent / KOH / 10 h / 130 °C

6.1: diethylazodicarboxylate; PPh₃ / benzene / 0.5 h / 20 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; PPA; boron tribromide; sodium carbonate; hydrazine hydrate; triphenylphosphine; diethylazodicarboxylate; diethylene glycol; In tetrahydrofuran; dichloromethane; toluene; xylene; benzene; 1.1: Cyclization / 2.1: Substitution / 3.1: demethylation / 4.1: Metallation / 4.2: Acylation / 5.1: Wolff-Kishner reduction / 5.2: Wolff-Kishner reduction / 6.1: Alkylation;
DOI:10.1021/jm990560c

Reference yield:

: 99-73-0,132309-76-3
para-bromophenacyl bromide

: 1027565-89-4
(S)-2-[4'-(2-Benzyl-benzofuran-3-yl)-biphenyl-4-yloxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: K₂CO₃ / acetone / 12 h / Heating

2.1: 74 percent / polyphosphoric acid / xylene / 12 h / Heating

3.1: 77 percent / Na₂CO₃; Pd(PPh₃)4 / toluene / 12 h / Heating

4.1: 87 percent / BBr₃ / CH₂Cl₂ / 10 h / 20 °C

5.1: n-BuLi / tetrahydrofuran / 3 h / -40 °C

5.2: 71 percent / tetrahydrofuran / 0.5 h / 0 °C

6.1: hydrazine monohydrate; diethylene glycol / 1 h / 180 °C

6.2: 94 percent / KOH / 10 h / 130 °C

7.1: diethylazodicarboxylate; PPh₃ / benzene / 0.5 h / 20 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; PPA; boron tribromide; sodium carbonate; potassium carbonate; hydrazine hydrate; triphenylphosphine; diethylazodicarboxylate; diethylene glycol; In tetrahydrofuran; dichloromethane; acetone; toluene; xylene; benzene; 1.1: Alkylation / 2.1: Cyclization / 3.1: Substitution / 4.1: demethylation / 5.1: Metallation / 5.2: Acylation / 6.1: Wolff-Kishner reduction / 6.2: Wolff-Kishner reduction / 7.1: Alkylation;
DOI:10.1021/jm990560c