4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

Base Information

Chemical Name:4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester
CAS No.:1025883-52-6
Molecular Formula:C₂₂H₂₅NO₃
Molecular Weight:351.445
Hs Code.:

Synonyms:4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

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Chemical Property of 4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

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Technology Process of 4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

There total 3 articles about 4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl 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: 91.0%

: 100-39-0
benzyl bromide

: 185501-26-2
4-(2-Methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

: 1025883-52-6
4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 85 ℃; for 4h;
DOI:10.1021/jm960486n

Reference yield:

: 1027657-18-6
4-(1-Acetyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid

: 1025883-52-6
4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂SO₄ / 15 h / Heating

2: 91 percent / K₂CO₃ / dimethylformamide / 4 h / 85 °C

With sulfuric acid; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm960486n

Reference yield:

: 131880-76-7
1-(2-methyl-2,3-dihydro-indol-1-yl)-ethanone

: 1025883-52-6
4-(1-Benzyl-2-methyl-2,3-dihydro-1H-indol-5-yl)-4-oxo-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: AlCl₃ / CH₂Cl₂ / 3 h / Heating

2: H₂SO₄ / 15 h / Heating

3: 91 percent / K₂CO₃ / dimethylformamide / 4 h / 85 °C

With aluminium trichloride; sulfuric acid; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm960486n