1429-05-6

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 85, p. 2446, 1963 DOI: 10.1021/ja00899a024

InChI:InChI=1/C13H9NO4/c15-13(18-12-4-2-1-3-5-12)10-6-8-11(9-7-10)14(16)17/h1-9H

Upstream product

• 122-04-3 4-nitro-benzoyl chloride 
• 108-95-2 phenol 
• 62-23-7 4-nitro-benzoic acid 
• 17954-26-6 1,2-dihydro-2-phenoxycarbonylisoquinoline-1-carbonitrile 
• 139-02-6 sodium phenoxide 
• 3847-57-2 sodium 4-nitrobenzoate 
• 1037-31-6 4-nitrophenyl 4-nitrobenzoate 
• 3229-70-7 phenolate 
• 7553-56-2 iodine 
• 71-43-2 benzene 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 13360-92-4 phenyl diphenylphosphinite 
• 164594-13-2 Phenyl[2-(trimethylsilyl)phenyl]iodonium trifluoromethanesulfonate 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 15850-20-1 4-nitro-N-(1,3-thiazol-2-yl)benzamide 
• 18920-70-2 4-hydroxy-4'-nitrobenzophenone 
• 68223-20-1 (2-hydroxyphenyl)(4-nitrophenyl)methanone 
• 36718-65-7 4-bromophenyl 4-nitrobenzoate 
• 10268-70-9 phenyl p-aminobenzoate 
• 34166-44-4 4,4'-azoxy-di-benzoic acid diphenyl ester 
• 33490-01-6 4-nitro-N-(2-nitrophenyl)benzamide 
• 3460-11-5 4-nitrobenzanilide 
• 139-29-7 N-(3-nitrophenyl)-4-nitro-benzamide 
• 64026-23-9 N-dodecyl-p-nitrobenzamide 
• 108-95-2 phenol 
• 55849-34-8 2-(p-Nitrobenzoyl)-1-indanon 
• 79859-22-6 4-(4-nitro-benzoyloxy)-benzoic acid methyl ester 
• 148964-72-1 4-[(4-octyloxybenzylidene)amino]benzoic acid phenyl ester 

Relevant academic research and scientific papers

Palladium/NHC-catalyzed tandem benzylic oxidation/oxidative esterification of benzylic alcohols with phenols

A palladium/NHC-catalyzed tandem benzylic oxidation/oxidative esterification of benzylic alcohols with phenols to access aryl benzoate derivatives is described. The procedure tolerates a series of functional groups, such as methoxy, nitro, cyano, chloro, fluoro and bromo groups. Thus, it represents a practically alternative method to access aryl benzoate derivatives.

Mechanically induced solvent-free esterification method at room temperature

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Br?nsted Acid Mediated Nucleophilic Functionalization of Amides through Stable Amide C?N Bond Cleavage; One-Step Synthesis of 2-Substituted Benzothiazoles

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Designing heterocyclic chalcones, benzoyl/sulfonyl hydrazones: An insight into their biological activities and molecular docking study

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Design and Bioevaluation of Novel Hydrazide-Hydrazones Derived from 4-Acetyl-N-Substituted Benzenesulfonamide

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We investigated the oxidative esterification of aldehydes with alcohols/phenols to produce a range of esters. In this approach, we conducted the reaction under metal-free conditions at room temperature. The reactions were promoted by potassium fluoride (KF) as the additive, resulting in the desired product in good to high yields. This procedure was found to be effective for the production of aryl esters, which are challenging in most of the available reports. It is vital for this procedure not to exclude air as the source of oxygen.

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