(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

Base Information

Chemical Name:(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one
CAS No.:1415686-18-8
Molecular Formula:C₂₇H₃₃NO₂Si
Molecular Weight:431.65
Hs Code.:

Synonyms:(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

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Chemical Property of (E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

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Technology Process of (E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

There total 6 articles about (E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one 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: 86.0%

: 13154-24-0
triisopropylsilyl chloride

: 1415686-24-6
(E)-3-(4-hydroxybenzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

: 1415686-18-8
(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/ol303036j

Reference yield: 57.0%

: 1415686-22-4
3-(4-((triisopropylsilyl)oxy)benzyl)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

: 1415686-18-8
(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; at 0 ℃; for 0.1h; Inert atmosphere;
DOI:10.1021/ol303036j

Reference yield:

: C₂₇H₃₂INO₂Si

: 1415686-18-8
(E)-3-(4-((triisopropylsilyl)oxy)benzylidene)-3,4-dihydrocyclopenta[b]indol-2(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / ethanol / 1.2 h / 20 °C

2: palladium diacetate; triphenylphosphine; triethylamine; formic acid / N,N-dimethyl-formamide / 6.5 h / 60 °C / Inert atmosphere

3: 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II) / acetone / 24 h / 60 °C / Inert atmosphere

With sodium tetrahydroborate; formic acid; 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II); palladium diacetate; triethylamine; triphenylphosphine; In ethanol; N,N-dimethyl-formamide; acetone; 2: |Heck Reaction / 3: |Oppenauer Oxidation;
DOI:10.1021/ol303036j