1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-one

Base Information

• Chemical Name: 1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-one
• CAS No.: 104061-74-7
• Molecular Formula: C14H10BrNO
• Molecular Weight: 288.143
• DSSTox Substance ID: DTXSID70707610
• Mol file: 104061-74-7.mol

Synonyms:104061-74-7;1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-one;DTXSID70707610

Chemical Property of 1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-one

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 286.99458
• Heavy Atom Count: 17
• Complexity: 290

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C(=O)C=CC2=CC=CC=N2)Br

Technology Process of 1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-one

There total 1 articles about 1-(2-Bromophenyl)-3-(pyridin-2-yl)prop-2-en-1-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: 50.0%

pyridine-2-carbaldehyde (1121-60-4) + 2-bromophenyl methyl ketone (2142-69-0) → 1-(2-bromophenyl)-3-(2-pyridinyl)-2-propen-1-one (104061-74-7)

Guidance literature:

With sodium hydroxide; In methanol; at 10 ℃; for 1.5h;

DOI:10.1021/jm00093a019

Reference yield:

1-(2-bromophenyl)-3-(2-pyridinyl)-2-propen-1-one (104061-74-7) → (+/-)-trans-3-(2-bromophenyl)octahydroindolizine (103729-18-6) + (+/-)-cis-3-(2-bromophenyl)octahydroindolizine (103729-18-6)

Guidance literature:

With hydrogen; acetic acid; Rh on carbon; for 72h; under 3102.9 Torr; Yield given. Yields of byproduct given;

DOI:10.1021/jm00093a019

Reference yield:

1-(2-bromophenyl)-3-(2-pyridinyl)-2-propen-1-one (104061-74-7) → (-)-(R)-trans-3-(2-bromophenyl)octahydroindolizine (103729-18-6)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂, glacial HOAc / 5percent Rh/C / 72 h / 3102.9 Torr

With hydrogen; acetic acid; Rh on carbon;

DOI:10.1021/jm00093a019

upstream raw materials:

pyridine-2-carbaldehyde

2-bromophenyl methyl ketone

Downstream raw materials:

(+/-)-trans-3-(2-bromophenyl)octahydroindolizine

(+/-)-cis-3-(2-bromophenyl)octahydroindolizine

(-)-(R)-trans-3-(2-bromophenyl)octahydroindolizine

(+)-(S)-trans-3-(2-bromophenyl)octahydroindolizine