(5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone

Base Information

• Chemical Name: (5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone
• CAS No.: 195253-51-1
• Molecular Formula: C17H13BrClNO
• Molecular Weight: 362.653
• DSSTox Substance ID: DTXSID20571303
• Mol file: 195253-51-1.mol

Synonyms:(5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone;195253-51-1;DTXSID20571303

Chemical Property of (5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone

Chemical Property:

• XLogP3: 5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 360.98690
• Heavy Atom Count: 21
• Complexity: 383

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1C=C(C2=C1C=CC(=C2)Br)C(=O)C3=CC=C(C=C3)Cl

Technology Process of (5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone

There total 2 articles about (5-Bromo-1-ethyl-1H-indol-3-yl)(4-chlorophenyl)methanone 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: 50.0%

4-chloro-benzoyl chloride (122-01-0) + 1-ethyl-5-bromo-1H-indole (195253-49-7) → (5-bromo-1-ethyl-1H-3-indolyl)(4-chlorophenyl)methanone (195253-51-1)

Guidance literature:

With aluminium trichloride; In dichloromethane; Heating;

DOI:10.1002/ardp.19973300506

Reference yield:

5-bromo-1H-indole (10075-50-0) → (5-bromo-1-ethyl-1H-3-indolyl)(4-chlorophenyl)methanone (195253-51-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 93 percent / NaH / dimethylformamide / 6 h / Heating

2: 50 percent / AlCl₃ / CH₂Cl₂ / Heating

With aluminium trichloride; sodium hydride; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1002/ardp.19973300506

Reference yield: 92.0%

(5-bromo-1-ethyl-1H-3-indolyl)(4-chlorophenyl)methanone (195253-51-1) → (5-bromo-1-ethyl-1H-3-indolyl)(4-chlorophenyl)methanol (195253-53-3)

Guidance literature:

With sodium tetrahydroborate; In methanol; Ambient temperature;

DOI:10.1002/ardp.19973300506

upstream raw materials:

4-chloro-benzoyl chloride

1-ethyl-5-bromo-1H-indole

5-bromo-1H-indole

Downstream raw materials:

(5-bromo-1-ethyl-1H-3-indolyl)(4-chlorophenyl)methanol