3-[2-(4-chlorophenyl)-2-oxoethyl]-3-hydroxy-1-methyl-1,3-dihydro-2H-indol-2-one

Base Information

• Chemical Name: 3-[2-(4-chlorophenyl)-2-oxoethyl]-3-hydroxy-1-methyl-1,3-dihydro-2H-indol-2-one
• CAS No.: 848-25-9
• Molecular Formula: C₁₇H₁₄ClNO₃
• Molecular Weight: 315.756
• Mol file: 848-25-9.mol

Synonyms:1-methyl-3-hydroxy-3-(2-(4-chlorophenyl)-2-oxoethyl)indolin-2-one

Chemical Property of 3-[2-(4-chlorophenyl)-2-oxoethyl]-3-hydroxy-1-methyl-1,3-dihydro-2H-indol-2-one

Chemical Property:

Purity/Quality:

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Technology Process of 3-[2-(4-chlorophenyl)-2-oxoethyl]-3-hydroxy-1-methyl-1,3-dihydro-2H-indol-2-one

There total 3 articles about 3-[2-(4-chlorophenyl)-2-oxoethyl]-3-hydroxy-1-methyl-1,3-dihydro-2H-indol-2-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: 83.0%

1-methyl-1H-indole-2,3-dione (2058-74-4) + para-chloroacetophenone (99-91-2) → 1-methyl-3-hydroxy-3-(2-(4-chlorophenyl)-2-oxoethyl)indolin-2-one (848-25-9)

Guidance literature:

With piperidine; In ethanol; at 20 ℃; for 6h;

DOI:10.002/cmdc.201402038

Reference yield:

indole-2,3-dione (91-56-5,1186480-61-4,84788-92-1) → 1-methyl-3-hydroxy-3-(2-(4-chlorophenyl)-2-oxoethyl)indolin-2-one (848-25-9)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

2: piperidine / ethanol / 6 h / 20 °C

With piperidine; potassium carbonate; In ethanol; N,N-dimethyl-formamide;

DOI:10.002/cmdc.201402038

Reference yield:

→ 1-methyl-3-hydroxy-3-(2-(4-chlorophenyl)-2-oxoethyl)indolin-2-one (848-25-9)

Guidance literature:

1-Methyl-2,3-dioxoindolin, 4-Chloracetophenon, ethanol. Diethylamin;

upstream raw materials:

1-methyl-1H-indole-2,3-dione

para-chloroacetophenone

indole-2,3-dione

Downstream raw materials:

1-methyl-3-(2-(4-chlorophenyl)-2-oxoethylidene)indolin-2-one

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