2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde

Base Information

• Chemical Name: 2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde
• CAS No.: 134903-47-2
• Molecular Formula: C₁₇H₁₄ClNO
• Molecular Weight: 283.757
• DSSTox Substance ID: DTXSID701215338
• Nikkaji Number: J2.786.689A

Synonyms:DTXSID701215338;AKOS005145415;134903-47-2;2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde

Chemical Property of 2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde

Chemical Property:

• XLogP3: 4.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 283.0763918
• Heavy Atom Count: 20
• Complexity: 329

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCN2C3=CC=CC=C3C(=C2Cl)C=O

Technology Process of 2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde

There total 1 articles about 2-Chloro-1-(2-phenylethyl)-1H-indole-3-carboxaldehyde 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: 85.0%

1-phenyl-2-bromoethane (103-63-9) + 2-chloroindole-3-carboxaldehyde (5059-30-3) → 2-chloro-N-(2-phenylethyl)indole-3-carbaldehyde (134903-47-2)

Guidance literature:

With potassium carbonate; In acetone; for 10h; Reflux;

DOI:10.1002/adsc.200900540

Reference yield: 82.0%

2-chloro-N-(2-phenylethyl)indole-3-carbaldehyde (134903-47-2) → C17H14INO (1213706-95-6)

Guidance literature:

With copper(l) iodide; potassium iodide; In N,N-dimethyl-formamide; at 120 ℃; for 48h;

DOI:10.1002/adsc.200900540

Reference yield: 72.0%

5-hydroxyoxindole (3416-18-0) + 2-chloro-N-(2-phenylethyl)indole-3-carbaldehyde (134903-47-2) → C25H19ClN2O2

Guidance literature:

With hydrogenchloride; In water; acetic acid; at 20 ℃; Reflux;

DOI:10.1016/j.ejmech.2014.04.004

upstream raw materials:

1-phenyl-2-bromoethane

2-chloroindole-3-carboxaldehyde

Downstream raw materials:

C₁₇H₁₄INO

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