1848-63-1

Upstream product

• 10349-38-9 p-methoxyphenylisonitrile 
• 141-43-5 ethanolamine 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 
• 104-94-9 4-methoxy-aniline 
• 5416-93-3 4-Methoxyphenyl isocyanate 
• 87919-18-4 1-(2-hydroxyethyl)-3-(4-methoxyphenyl)urea 
• 1848-60-8 1-(2-hydroxyethyl)-3-(4-methoxyphenyl)thiourea 
• 1227-45-8 1,3-bis-(p-methoxyphenyl)thiourea 
• 65536-40-5 N-(2-chloro-ethyl)-N'-(4-methoxy-phenyl)-urea 

Relevant academic research and scientific papers

Synthesis of 2-aminooxazolines from isonitriles and iodine

A novel one-pot protocol for the synthesis of substituted 2-aminooxazoline from isonitriles and 2-aminoethanol was developed and the reactions involved imidoyl diiodide intermediates, which were generated by mixing isonitriles and iodine in CH2

Investigation of the Mitsunobu reaction of N-(2-hydroxyethyl)-N'- phenyl-ureas

The Mitsunobu reaction of N-(2-hydroxyethyl)-ureas 1 using PPh3 and EtO2CN=NCO2Et led to the mixture of N- and O-alkylation products or a single isomer depending on the substrates.

Efficient Cyclodesulfurization of N-(2-Hydroxyethyl)-N′-Arylthioureas to Δ2-Oxazolines Using Superoxide Radical Anion

Δ2-Oxazolines have been synthesized in good yields by the cyclodesulfurization of N-(2-hydroxyethyl)-N′-phenylthioureas with superoxide radical anion (O2-?) at room temperature in anhydrous acetonitrile.