methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

Base Information

Chemical Name:methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate
CAS No.:923584-42-3
Molecular Formula:C₃₂H₂₇Cl₂NO₃
Molecular Weight:544.477
Hs Code.:

Synonyms:methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

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Chemical Property of methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

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Technology Process of methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

There total 6 articles about methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate 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: 28.0%

: 872674-87-8
3-(2-bromoethyl)-5-chloro-1-(diphenylmethyl)-2-methyl-1H-indole

: 3964-57-6
methyl 4-hydroxy-3-chlorobenzoate

: 923584-42-3
methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

Guidance literature:: methyl 4-hydroxy-3-chlorobenzoate; With sodium hydride; In dimethyl sulfoxide; for 0.25h;

3-(2-bromoethyl)-5-chloro-1-(diphenylmethyl)-2-methyl-1H-indole; In dimethyl sulfoxide; at 80 ℃; for 18h;
DOI:10.1021/jm0507882

Reference yield:

: 4-[(4-chloro-phenyl)-hydrazono]-pentanoic acid ethyl ester

: 923584-42-3
methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: ZnCl₂ / 140 °C

2.1: NaH / dimethylformamide / 0.5 h / 0 °C

2.2: 17 percent / dimethylformamide / 0 - 20 °C

3.1: LiAlH₄ / tetrahydrofuran / 0.5 h / 10 °C

4.1: 76 percent / 1,3-bis(diphenylphosphino)propane; carbon tetrabromide / CH₂Cl₂ / 0 - 20 °C

5.1: NaH / dimethylsulfoxide / 0.25 h

5.2: 28 percent / dimethylsulfoxide / 18 h / 80 °C

With lithium aluminium tetrahydride; carbon tetrabromide; 1,3-bis-(diphenylphosphino)propane; sodium hydride; zinc(II) chloride; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 1.1: Fisher indole synthesis;
DOI:10.1021/jm0507882

Reference yield:

: 479422-74-7
2-(1-benzhydryl-5-chloro-2-methyl-1H-indol-3-yl)ethanol

: 923584-42-3
methyl 3-chloro-4-[2-[5-chloro-1-(diphenylmethyl)-2-methyl-1H-indol-3-yl]ethoxy]benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: 76 percent / 1,3-bis(diphenylphosphino)propane; carbon tetrabromide / CH₂Cl₂ / 0 - 20 °C

2.1: NaH / dimethylsulfoxide / 0.25 h

2.2: 28 percent / dimethylsulfoxide / 18 h / 80 °C

With carbon tetrabromide; 1,3-bis-(diphenylphosphino)propane; sodium hydride; In dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm0507882