59101-32-5

Upstream product

• 10507-69-4 4-methoxybenzohydroxamic acid 
• 98-88-4 benzoyl chloride 
• 108-90-7 chlorobenzene 
• 60-29-7 diethyl ether 
• 532-31-0 silver benzoate 
• 38435-51-7 N-hydroxy-4-methoxy-benzenecarboximidoyl chloride 
• 7647-01-0 hydrogenchloride 
• 100-09-4 4-methoxybenzoic acid 
• 860584-94-7 (+/-)-4-(chloro-nitroso-methyl)-anisole 
• 94-36-0 dibenzoyl peroxide 
• 3717-21-3 (E)-4-methoxybenzaldoxime 
• 3717-22-4 (Z)-para-methoxybenzaldehyde oxime 
• 100-07-2 4-methoxy-benzoyl chloride 
• 57139-22-7 potassium p-methoxylbenzohydroxamate 

Downstream Products

• 5416-93-3 4-Methoxyphenyl isocyanate 
• 7472-54-0 N-(p-methoxyphenyl)benzamide 
• 104-94-9 4-methoxy-aniline 
• 10507-69-4 4-methoxybenzohydroxamic acid 
• 65-85-0 benzoic acid 
• 124-38-9 carbon dioxide 
• 1227-44-7 N,N'-bis(4-methoxyphenyl)urea 

Relevant academic research and scientific papers

A very mild and selective method for O-benzoylation of hydroxamic acids

Selective O-benzoylation of hydroxamic acids is achieved by the treatment of BPO and DABCO. Aliphatic alcohols are not reactive under these conditions. Various radical or oxidation sensitive functional groups are compatible with this protocol, and no anhydrous reagents or solvents are required for the high yields of the benzoylations.

Regio-selective formation of O-acyl/O-benzoyl hydroxamates by using a polymer supported reagent strategy

Rapid, quantitative and regioselective O-acylation/O-benzoylation of hydroxamic acids has been carried using polymer supported hydroxamate anions and acetyl/benzoyl chloride under mild conditions. The isolation of unambiguous and pure products by si-mple

PREPARATION AND CHARACTERIZATION OF MIXED ANHYDRIDES OF O-ACYLARYLCARBOHYDROXIMIC ACID

A number of N,O-diacylhydroxylamines have been prepared by the reaction of potassium salts of hydroxamic acids with a variety of acylating agents which include: benzoyl, p-nitrobenzoyl, anisoyl, p-chlorobenzoyl and lauroyl chlorides in dioxane under reflu