1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole

Base Information

• Chemical Name: 1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole
• CAS No.: 67060-93-9
• Molecular Formula: C13H13NO
• Molecular Weight: 199.252
• DSSTox Substance ID: DTXSID30397738
• Nikkaji Number: J519.341I
• Wikidata: Q82199310

Synonyms:1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole;ST50983592;67060-93-9;DTXSID30397738;HMS1608J09;AKOS001612979;NCGC00336774-01;2-(4-methoxyphenyl)-1-vinyl-1H-pyrrole;AB01330586-02;AB01330586-03;SR-01000404140;SR-01000404140-1;InChI=1/C13H13NO/c1-3-14-10-4-5-13(14)11-6-8-12(15-2)9-7-11/h3-10H,1H2,2H

Chemical Property of 1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole

Chemical Property:

• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 199.099714038
• Heavy Atom Count: 15
• Complexity: 209

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C2=CC=CN2C=C

Technology Process of 1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole

There total 2 articles about 1-Vinyl-2-(4-methoxyphenyl)-1H-pyrrole 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:

1-(4-methoxyphenyl)ethanone (100-06-1) → 2-(4-methoxyphenyl)-1H-pyrrole (4995-12-4) + 2-(4-methoxyphenyl)-1-vinylpyrrole (67060-93-9)

Guidance literature:

Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride

2: water; potassium hydroxide; 18-crown-6 ether / dimethyl sulfoxide / 15 h / 100 °C / Sealed tube; Green chemistry

With 18-crown-6 ether; hydroxylamine hydrochloride; water; potassium hydroxide; In dimethyl sulfoxide;

DOI:10.1039/c4gc01615g

Reference yield:

→ 2-(4-methoxyphenyl)-1-vinylpyrrole (67060-93-9)

Guidance literature:

p-Methoxyacetophenon-oxim, Acetylen, KOH, DMSO, Autoklav;

DOI:10.1007/BF00472152

Reference yield: 94.0%

2-(4-methoxyphenyl)-1-vinylpyrrole (67060-93-9) + ethenetetracarbonitrile (670-54-2) → 3-[2-(4-methoxyphenyl)-1H-pyrrol-1-yl]-1,1,2,2-cyclobutanetetracarbonitrile (1167431-29-9)

Guidance literature:

In acetone; at 20 ℃; for 1h; regiospecific reaction;

DOI:10.1016/j.tet.2009.03.094

upstream raw materials:

1-(4-methoxyphenyl)ethanone

Downstream raw materials:

1-Vinyl-2-(p-methoxy)phenyl-5-trifluoracetylpyrrol

5-(4-methoxyphenyl)-1H-pyrrole-2-carbaldehyde

(3E)-4-[2-(4-methoxyphenyl)-1H-pyrrol-1-yl]-1,3-butadiene-1,1,2-tricarbonitrile

3-[2-(4-methoxyphenyl)-1H-pyrrol-1-yl]-1,1,2,2-cyclobutanetetracarbonitrile

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