2-phenyl-6,7-dihydro-1H-indol-4(5H)-one

Base Information

• Chemical Name: 2-phenyl-6,7-dihydro-1H-indol-4(5H)-one
• CAS No.: 14006-77-0
• Molecular Formula: C10H11NO3
• Molecular Weight: 211.263
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID60473776
• Nikkaji Number: J276.697C
• Wikidata: Q82303397
• Mol file: 14006-77-0.mol

Synonyms:2-phenyl-6,7-dihydro-1H-indol-4(5H)-one;14006-77-0;2-Phenyl-6,7-dihydroindol-4(5H)-one;2-phenyl-1,5,6,7-tetrahydroindol-4-one;SCHEMBL11394395;SCHEMBL11394400;DTXSID60473776;IOCKGQRVMMIOHM-UHFFFAOYSA-N;MFCD18911039;SY298754;4-oxo-2-phenyl-4,5,6,7-tetrahydroindole;2-Phenyl-1,5,6,7-tetrahydro-4H-indol-4-one

Chemical Property of 2-phenyl-6,7-dihydro-1H-indol-4(5H)-one

Chemical Property:

• PSA: 32.86000
• LogP: 3.20070
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 211.099714038
• Heavy Atom Count: 16
• Complexity: 270

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2=C(C=C(N2)C3=CC=CC=C3)C(=O)C1

Technology Process of 2-phenyl-6,7-dihydro-1H-indol-4(5H)-one

There total 16 articles about 2-phenyl-6,7-dihydro-1H-indol-4(5H)-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: 89.0%

2-oxo-1-(6-oxocyclohex-1-en-1-yl)-2-phenylethyl acetate (1380499-39-7) → 2-phenyl-1,5,6,7-tetrahydro-4H-indol-4-one (14006-77-0)

Guidance literature:

With ammonia; In methanol; at 20 ℃; for 0.166667h;

DOI:10.1002/ejoc.201200107

Reference yield: 84.0%

1,5,6,7-tetrahydro-indol-4-one (13754-86-4) + diphenyliodonium tetrafluoroborate → 2-phenyl-1,5,6,7-tetrahydro-4H-indol-4-one (14006-77-0)

Guidance literature:

With palladium; In tetrahydrofuran; at 60 ℃; for 24h;

DOI:10.1039/d0cc06716d

Reference yield: 70.0%

3-amino-cyclohex-2-enone (5220-49-5) + α-bromoacetophenone (70-11-1) → 2-phenyl-1,5,6,7-tetrahydro-4H-indol-4-one (14006-77-0)

Guidance literature:

With boron trifluoride diethyl etherate; In dichloromethane; at 130 ℃; for 0.216667h; Reagent/catalyst; Solvent; Microwave irradiation;

DOI:10.1007/s11164-015-1966-9

upstream raw materials:

3-amino-cyclohex-2-enone

α-bromoacetophenone

N-<(3-oxo-2-cyclohexenyl)imino>triphenylphosphorane

2-phenacylcyclohexane-1,3-dione

Downstream raw materials:

2-phenylpyrrolo<2,3-c>carbazole