(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

Base Information

Chemical Name:(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester
CAS No.:1026557-63-0
Molecular Formula:C₃₇H₂₉NO₆
Molecular Weight:583.64
Hs Code.:

Synonyms:(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

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Chemical Property of (R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

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Technology Process of (R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

There total 9 articles about (R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic 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:

: 13673-95-5
(S)-methyl 2-hydroxy-3-phenylpropanoate

: 250279-12-0
4'-(2-benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-ol

: 1026557-63-0
(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic 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

: 1026557-63-0
(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 7 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: iron(III) nitrate nonahydrate / ethanol / 1.5 h / 45 °C

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

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; PPA; boron tribromide; sodium carbonate; hydrazine hydrate; ferric nitrate; triphenylphosphine; diethylazodicarboxylate; diethylene glycol; In tetrahydrofuran; ethanol; 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: Nitration / 7.1: Alkylation;
DOI:10.1021/jm990560c

Reference yield:

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

: 1026557-63-0
(R)-2-[4'-(2-Benzyl-benzofuran-3-yl)-3-nitro-biphenyl-4-yloxy]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 8 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: iron(III) nitrate nonahydrate / ethanol / 1.5 h / 45 °C

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

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; PPA; boron tribromide; sodium carbonate; potassium carbonate; hydrazine hydrate; ferric nitrate; triphenylphosphine; diethylazodicarboxylate; diethylene glycol; In tetrahydrofuran; ethanol; 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: Nitration / 8.1: Alkylation;
DOI:10.1021/jm990560c