14546-38-4Relevant articles and documents
Expeditious and Efficient ortho-Selective Trifluoromethane-sulfonylation of Arylhydroxylamines
Liu, Yue,Bai, Songlin,Du, Yuanbo,Qi, Xiangbing,Gao, Hongyin
supporting information, (2021/12/27)
A metal- and oxidant-free, practical and efficient method for the synthesis of highly versatile and synthetically useful ortho-trifluoromethanesulfonylated anilines from arylhydroxylamines and trifluoromethanesulfinic chloride was developed. This rapid tr
Preparation, properties and infrared spectral studies of N-(p-ethylphenyl)thiobenzohydroxamic acid
Kakkar, Rita,Dua, Amita,Zaidi, Sheza
, p. 1362 - 1369 (2008/09/17)
The preparation of N-(p-ethylphenyl)thiobenzohydroxamic acid and its spectral properties are described in this paper. The preferred conformation of the acid is investigated by both infrared techniques and theoretical calculations at the DFT level. It is f
Method for producing 5-substituted-2-acylaminophenols, and 5-alkyl-2-acylaminophenol compound and N-acyl-N-(4-alkyl-phenyl)hydroxylamine compound
-
, (2008/06/13)
There is disclosed a method for producing 5-substituted-2-acylaminophenols of formula (I), comprising hydrolyzing to partially deacylate a compound of formula (V): ???in formulae (I) and (V), R1represents an aliphatic hydrocarbon group, an aliphatic hydrocarbon oxy group, an aryloxy group, an acylamino group, a disubstituted amino group, or a hydroxyl group; R2represents an acyl group; X1and X2each represent a hydrogen atom or a halogen atom; and R3represents an acyl group. According to the present invention, a method for synthesizing 2-acylaminophenols that uses inexpensive starting materials, has short steps, is environmentally friendly, is high in safety, and is low in cost, is provided.