2-(Phenylsulfinyl)-1H-indole

Base Information

Chemical Name:2-(Phenylsulfinyl)-1H-indole
CAS No.:169890-97-5
Molecular Formula:C₁₄H₁₁NOS
Molecular Weight:241.313
Hs Code.:

Synonyms:2-(Phenylsulfinyl)-1H-indole

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Chemical Property of 2-(Phenylsulfinyl)-1H-indole

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Technology Process of 2-(Phenylsulfinyl)-1H-indole

There total 3 articles about 2-(Phenylsulfinyl)-1H-indole 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%

: 120517-31-9
5-chloro-2-(methylthio)-1H-indole

: 169890-97-5
2-(Phenylsulfinyl)-1H-indole

Guidance literature:: With potassium peroxymonosulfate sulfate; In tetrahydrofuran; methanol; at -20 - 0 ℃; for 10h;
DOI:10.1002/adsc.202000308

Reference yield:

: 59-48-3
2-oxoindole

: 169890-97-5
2-(Phenylsulfinyl)-1H-indole

Guidance literature:: Multi-step reaction with 3 steps

1: Lawessons reagent / toluene / Inert atmosphere; Reflux; Schlenk technique

2: cesium fluoride / acetonitrile / 4 h / 70 °C / Inert atmosphere; Schlenk technique

3: potassium peroxymonosulfate sulfate / tetrahydrofuran; methanol / 10 h / -20 - 0 °C

With Lawessons reagent; potassium peroxymonosulfate sulfate; cesium fluoride; In tetrahydrofuran; methanol; toluene; acetonitrile;
DOI:10.1002/adsc.202000308

Reference yield:

: 496-30-0
indolin-2-thione

: 169890-97-5
2-(Phenylsulfinyl)-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: cesium fluoride / acetonitrile / 4 h / 70 °C / Inert atmosphere; Schlenk technique

2: potassium peroxymonosulfate sulfate / tetrahydrofuran; methanol / 10 h / -20 - 0 °C

With potassium peroxymonosulfate sulfate; cesium fluoride; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1002/adsc.202000308