98061-62-2

Upstream product

• 14476-72-3 2-(2-oxo-2-phenylethyl)malononitrile 
• 22109-04-2 2-amino-3-cyano-5-phenyl-4,5-dihydrofuran 
• 1674-30-2 1-phenyl-2-chloroethanol 
• 96-09-3 styrene oxide 
• 98-88-4 benzoyl chloride 
• 14742-32-6 2-amino-5-phenylfuran-3-carbonitrile 
• 98061-59-7 2-benzamido-3-cyano-5-phenyl-4,5-dihydrofuran 

Downstream Products

• 1253900-97-8 N-(3-cyano-5-phenyl-2-furanyl)-N-4-penten-1-ylbenzamide 
• 1253900-81-0 N-3-buten-1-yl-N-(3-cyano-5-phenyl-2-furanyl)benzamide 

Relevant academic research and scientific papers

Synthesis of dihydroindoles and tetrahydroquinolines by the intramolecular diels-alder reaction of N-alkenylated 2-acylamino-3-furancarbonitriles

An approach to dihydroindoles and tetrahydroquinolines from N-alkenylated 2-acylamino-3-furancarbonitriles via a [4 + 2] cycloaddition reaction is described. Thermal treatment of N-alkenylated 2-acylamino-3-furancarbonitriles 5ad, 6ad, 9ad, and 10ad, whic

Studies on Heterocyclic Enaminonitriles. VI. Synthesis of 2-Amino-3-cyano-4,5-dihydrofurans

Malononitrile reacts with 2-chloroethanol and 1-chloro-2-propanol (or 2-methyloxirane) in the presence of sodium ethoxide to give 2-amino-3-cyano-4,5-dihydrofuran (Ia) and 2-amino-3-cyano-5-methyl-4,5-dihydrofuran (Ib), respectively.The reaction of malono