88803-91-2

Upstream product

• 5663-67-2 2-acetoxybenzaldehyde 
• 50-78-2 aspirin 
• 5538-51-2 O-acetylsalicyloyl chloride 

Downstream Products

• 126430-19-1 2-Acetoxy-benzoic acid (2S,5R)-5-(4-acetylamino-2-oxo-2H-pyrimidin-1-yl)-2,5-dihydro-furan-2-ylmethyl ester 
• 126430-17-9 2-Acetoxy-benzoic acid (2R,3R,4S,5R)-3-acetoxy-5-(4-acetylamino-2-oxo-2H-pyrimidin-1-yl)-4-bromo-tetrahydro-furan-2-ylmethyl ester 
• 126430-16-8 2-Acetoxy-benzoic acid (2R,3S,4S,5R)-4-acetoxy-5-(4-acetylamino-2-oxo-2H-pyrimidin-1-yl)-3-bromo-tetrahydro-furan-2-ylmethyl ester 
• 41390-40-3 2-[(cyclohexylamino)carbonyl]phenyl acetate 
• 126430-21-5 2-Acetoxy-benzoic acid (2S,5R)-5-(4-acetylamino-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester 

Relevant academic research and scientific papers

A mild and efficient reaction for conversion of carboxylic acids into acid bromides with ethyl tribromoacetate/triphenylphosphine under acid-free conditions

Acid bromides were prepared efficiently from carboxylic acids with readily available ethyl tribromoacetate and triphenylphosphine at room temperature under neutral conditions. The present process is applicable to the preparation of various acid bromides from aromatic and aliphatic carboxylic acids. Aromatic carboxylic acids were found to be more reactive than aliphatic carboxylic acids under reaction conditions.