{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

Base Information

Chemical Name:{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester
CAS No.:1471996-69-6
Molecular Formula:C₃₀H₂₉NO₄
Molecular Weight:467.565
Hs Code.:

Synonyms:{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

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Chemical Property of {(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

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Technology Process of {(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

There total 6 articles about {(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic 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:

: 1471996-62-9
methyl 2-((S)-6-((R)-4-bromo-5-cyano-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate

: 83902-02-7
2,6-dimethylbenzyl bromide

: 1471996-69-6
{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

Guidance literature:: 2,6-dimethylbenzyl bromide; With chloro-trimethyl-silane; ethylene dibromide; lithium chloride; zinc; In tetrahydrofuran; for 0.5h; Inert atmosphere;

methyl 2-((S)-6-((R)-4-bromo-5-cyano-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate; With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; In tetrahydrofuran; at 60 ℃; Inert atmosphere;

Reference yield:

: 1471996-61-8
(S)-4-bromo-1-hydroxy-2,3-dihydro-1H-indene-5-carbonitrile

: 1471996-69-6
{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: di-tert-butyl-diazodicarboxylate; tributylphosphine / tetrahydrofuran / 1.25 h / -10 °C

2.1: lithium chloride; zinc; ethylene dibromide; chloro-trimethyl-silane / tetrahydrofuran / 0.5 h / Inert atmosphere

2.2: 60 °C / Inert atmosphere

With chloro-trimethyl-silane; tributylphosphine; di-tert-butyl-diazodicarboxylate; ethylene dibromide; lithium chloride; zinc; In tetrahydrofuran;

Reference yield:

: 896132-97-1
4-bromo-5-hydroxy-2,3-dihydro-1H-inden-1-one

: 1471996-69-6
{(S)-6-[(R)-5-cyano-4-(2,6-dimethyl-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 - 20 °C

2.1: 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / N,N-dimethyl-formamide / 1 h / 70 °C / Inert atmosphere

3.1: formic acid; triethylamine; chloro([(S,2S)-(?)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido)(mesitylene)ruthenium (II) / dichloromethane / 2 h / 20 °C / Inert atmosphere

4.1: di-tert-butyl-diazodicarboxylate; tributylphosphine / tetrahydrofuran / 1.25 h / -10 °C

5.1: lithium chloride; zinc; ethylene dibromide; chloro-trimethyl-silane / tetrahydrofuran / 0.5 h / Inert atmosphere

5.2: 60 °C / Inert atmosphere

With 2,6-dimethylpyridine; 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; chloro([(S,2S)-(?)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido)(mesitylene)ruthenium (II); chloro-trimethyl-silane; formic acid; tributylphosphine; di-tert-butyl-diazodicarboxylate; ethylene dibromide; triethylamine; lithium chloride; zinc; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;