2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)-

Base Information

• Chemical Name: 2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)-
• CAS No.: 282549-39-7
• Molecular Formula: C16H15NO
• Molecular Weight: 237.29600
• DSSTox Substance ID: DTXSID60475710
• Nikkaji Number: J1.738.026E
• Mol file: 282549-39-7.mol

Synonyms:2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)-;282549-39-7;3-(2-PHENYLETHYL)-1,3-DIHYDROINDOL-2-ONE;3-(2-Phenylethyl)-1,3-dihydro-2H-indol-2-one;DTXSID60475710

Chemical Property of 2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)-

Chemical Property:

• PSA: 32.59000
• LogP: 3.44020
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 237.115364102
• Heavy Atom Count: 18
• Complexity: 296

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCC2C3=CC=CC=C3NC2=O

Technology Process of 2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)-

There total 4 articles about 2H-Indol-2-one, 1,3-dihydro-3-(2-phenylethyl)- 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: 90.0%

2-oxoindole (59-48-3) + 2-phenylethanol (60-12-8) → 3-phenethylindolin-2-one (282549-39-7)

Guidance literature:

In 1,3,5-trimethyl-benzene; at 170 ℃; for 24h; Inert atmosphere;

DOI:10.1039/c3cy00911d

Reference yield: 84.0%

3-phenylacetyl-indolin-2-one (103585-66-6) → 3-phenethylindolin-2-one (282549-39-7)

Guidance literature:

With sodium tetrahydroborate; acetic acid; at 75 ℃; for 1h;

DOI:10.1080/00397910500449583

Reference yield:

(E)-N-(2-(3-phenylprop-1-en-1-yl)phenyl)formamide (1536478-65-5) → 3-phenethylindolin-2-one (282549-39-7) + 3-benzyl-3,4-dihydro-1H-quinolin-2-one (1137992-05-2)

Guidance literature:

With dodecacarbonyl-triangulo-triruthenium; tetra-(n-butyl)ammonium iodide; In dimethyl sulfoxide; toluene; at 20 - 120 ℃; for 20.08h; Overall yield = 84 %Spectr.; regioselective reaction; Sealed tube;

DOI:10.1021/ja411913e

upstream raw materials:

3-phenylacetyl-indolin-2-one

N-(2-bromophenyl)formamide

[(1E)-3-phenylprop-1-en-1-yl]boronic acid

(E)-N-(2-(3-phenylprop-1-en-1-yl)phenyl)formamide