613-78-5Relevant academic research and scientific papers
Synthesis of salicylates from anionically activated aromatic trifluoromethyl group
Lin, Chuankai,Liu, Jin-Biao,Wang, Ruixiang,Xie, Huilin
supporting information, (2021/12/22)
An efficient approach to salicylates via a novel transformation of anionically activated aromatic trifluoromethyl group is described. Anionically activated trifluoromethyl group can react with phenols/alcohols under alkaline conditions to afford aryl/alkyl salicylates in high yields. Mechanism studies indicate that the carbonyl oxygen atom of ester is from the H2O in the solvent.
Supramolecular Pd(II) complex of DPPF and dithiolate: An efficient catalyst for amino and phenoxycarbonylation using Co2(CO)8 as sustainable C1 source
Gaikwad, Vinayak V.,Mane, Pravin A.,Dey, Sandip,Patel, Divya,Bhanage, Bhalchandra M.
, (2019/11/28)
Highly active, efficient and robust “dppf ligated tetranuclear palladium dithiolate complex” was synthesized and applied as a catalyst for chemical fixation of carbon monoxide for the synthesis value added chemicals such as tertiary amide and aromatic esters. The synthesized catalyst was characterized using different analytical techniques such as elemental analysis, 1H and 31P NMR spectroscopy. The use of Co2(CO)8 as a cheap, less toxic and low melting solid surrogate are additional advantages over the current protocol. The catalyst showed superior activity towards the Amino (10?3 mol % catalyst) and Phenoxycarbonylation (10-2 mol % catalyst) and high TON (104 to 103) and TOF (103 to 102 h-1). The Betol and Lintrin (active drug molecules) were synthesized under an optimized reaction condition. The scalability of the current protocol has been demonstrated up-to the gram level.
A photoredox-neutral Smiles rearrangement of 2-aryloxybenzoic acids
Gonzalez-Gomez, Jose C.,Ramirez, Nieves P.,Lana-Villarreal, Teresa,Bonete, Pedro
, p. 9680 - 9684 (2017/11/30)
We report on the use of visible light photoredox catalysis for the radical Smiles rearrangement of 2-aryloxybenzoic acids to obtain aryl salicylates. The method is free of noble metals and operationally simple and the reaction can be run under mild batch or flow conditions. Being a redox neutral process, no stoichiometric oxidants or reductants are needed.
Carboxyl radical-assisted 1,5-aryl migration through Smiles rearrangement
Hossian, Asik,Jana, Ranjan
supporting information, p. 9768 - 9779 (2016/10/31)
We report herein, a silver(i)-catalyzed Smiles rearrangement of 2-aryloxy- or 2-(arylthio)benzoic acids to provide aryl-2-hydroxybenzoate or aryl-2-mercaptobenzoate dimer, respectively, through 1,5-aryl migration from oxygen or sulfur to carboxylate oxygen. Mechanistically, the aryl ether moiety undergoes an intramolecular ipso attack by the carboxyl radical followed by a C-O or C-S bond cleavage. Aryl-2-mercaptobenzoates undergo oxidative dimerization through a thiol moiety in situ.
Acylation of Phenols with Salicylic Acid Using Polyphosphoric Acid
Kamat, S. P.,Paknikar, S. K.
, p. 773 - 774 (2007/10/02)
Acylation of 2-naphthol (2), 1-naphthol (6) and resorcinol (11) with salicylic acid (1) in the presence of PPA affords salicylate esters (4, 7, 13 and 14), 1,2-benzoxanthone (5), 3,4-benzoxanthone (8), 3-hydroxyxanthone (12), 2-salicoyl-1-naphthol (9) and 11-hydroxy-12H-benzoxanthen-12-one (10).Compounds (4, 5, 7, 8, 12, 13 and 14) are identical with those obtained by heating a mixture of phenyl salicylate (3) and phenols (2, 6 and 11).
Thermal Conversion of Salol into Xanthone: A Mechanistic Study
Kamat, S. P.,Paknikar, S. K.
, p. 38 - 41 (2007/10/02)
The thermal conversion of salol (1) into xanthone has been rationalized as proceeding via the keto-ketene intermediate (7) which is trapped by phenols (9, 12 and 15).
