tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate
CAS No.:1207869-12-2
Molecular Formula:C₂₈H₂₆ClNO₅
Molecular Weight:491.971
Hs Code.:

Synonyms:tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

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Chemical Property of tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

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Technology Process of tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

There total 5 articles about tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate 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:

: C₃₂H₃₇NO₅Si

: 1207869-12-2
tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2012.09.048

Reference yield:

: 67-36-7
4-phenoxy benzaldehyde

: 1207869-12-2
tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: carbon dioxide; n-butyllithium / tetrahydrofuran; hexane / 2 h / -78 - 20 °C / Inert atmosphere

1.2: 1 h / -78 °C / Inert atmosphere

1.3: 1 h / -78 - 20 °C / Inert atmosphere

2.1: manganese(IV) oxide / acetone / 20 °C / Inert atmosphere

3.1: dmap / tetrahydrofuran; hexane / 1 h / 20 °C / Inert atmosphere

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

5.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C / Inert atmosphere

With dmap; manganese(IV) oxide; n-butyllithium; carbon dioxide; tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmc.2012.09.048

Reference yield:

: 1411975-46-6
(4-(tert-butyldimethylsilyloxy)-1H-indol-2-yl)(4-phenoxyphenyl)methanone

: 1207869-12-2
tert-butyl 4-(2-chloroethoxy)-2-(4-phenoxybenzoyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: dmap / tetrahydrofuran; hexane / 1 h / 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C / Inert atmosphere

With dmap; tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2012.09.048