1-(Methoxymethyl)-1H-pyrrole

Base Information

• Chemical Name: 1-(Methoxymethyl)-1H-pyrrole
• CAS No.: 76322-78-6
• Molecular Formula: C₆H₉NO
• Molecular Weight: 111.144
• Hs Code.: 2933998090
• European Community (EC) Number: 877-529-6

Synonyms:1-(Methoxymethyl)-1H-pyrrole;1-(Methoxymethyl)pyrrole;76322-78-6;SCHEMBL4473832;BDA32278;AKOS014313945;BS-32777;CS-0210401;EN300-216194

Chemical Property of 1-(Methoxymethyl)-1H-pyrrole

Chemical Property:

• XLogP3: 0.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 111.068413911
• Heavy Atom Count: 8
• Complexity: 59.5

Purity/Quality:

99% ^*data from raw suppliers

1-(Methoxymethyl)pyrrole 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COCN1C=CC=C1

Technology Process of 1-(Methoxymethyl)-1H-pyrrole

There total 2 articles about 1-(Methoxymethyl)-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:

pyrrole (109-97-7,30604-81-0) + chloromethyl methyl ether (107-30-2) → 1-(methoxymethyl)pyrrole (76322-78-6)

Guidance literature:

With sodium hydride; Yield given. Multistep reaction; 1.) DMF, 0 deg C, 2 h, 2.) 15 deg C, 6 h;

DOI:10.1055/s-1986-31722

Reference yield:

→ 1-(methoxymethyl)pyrrole (76322-78-6)

Guidance literature:

Reference yield:

methyl 2-chloro-5-(1H-pyrazol-4-yl)benzoate + 1-(methoxymethyl)pyrrole (76322-78-6) → methyl 2-chloro-5-[1-[1-(methoxymethyl)pyrrol-2-yl]pyrazol-4-yl]benzoate

Guidance literature:

With sodium hypochlorite; sodium hydrogencarbonate; In water; acetonitrile; at 30 - 35 ℃; for 1h;

upstream raw materials:

pyrrole

chloromethyl methyl ether

Downstream raw materials:

ethyl 1-methoxymethyl-4-aminopyrrole-2-carboxylate

1-(methoxymethyl)-4-nitropyrrole-2-carboxylic acid

1-Methoxymethyl-2-((E)-styryl)-1H-pyrrole

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