Synthesis of 3-Amino-5-fluoroalkylfurans by Intramolecular Cyclization was written by Placais, Clotilde;Donnard, Morgan;Panossian, Armen;Vors, Jean-Pierre;Bernier, David;Pazenok, Sergii;Leroux, Frederic R.. And the article was included in Organic Letters in 2021.Recommanded Product: 109-85-3 The following contents are mentioned in the article:
A synthesis to access rarely described 3-amino-5-fluoroalkylfurans has been developed by cyclization of easily accessible fluorovinamides. This method is rapid and simple and affords the desired furans as hydrochloride salts in quant. or nearly quant. yields. It is compatible with four different fluorinated groups (-CF3, -CF2CF3, -CHF2, and -CF2Cl) and a wide range of substituents on the amine. This study involved multiple reactions and reactants, such as 2-Methoxyethylamine (cas: 109-85-3Recommanded Product: 109-85-3).
2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 109-85-3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem