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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353763Generated: October 31, 2026

5-Aminosalicylic Acid → 5-Benzylaminosalicylic acid

https://huagongshe.com/reaction/2353763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminosalicylic AcidHCID 4075—
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
Product5-Benzylaminosalicylic acidHCID 9899588113.8%

Reaction Steps

To a solution of 5-aminosalicylic acid (2.0 g, 13 mmole, purchased from Aldrich Chemical Company, USA) and triethylamine in dried DMF (25 ml) was added benzyl bromide (2.68 g, 1.90 ml, 15.6 mmole) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred for 4 hr at room temperature. Ice chips were added to the reaction mixture and then solvent was removed in vacuo. The reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous MgSO4. After evaporation of the solvent, the residue was purified by column chromatography and recrystallized from methanol/ethyl acetate/hexane (1:3:1) to give 3.6 g (73% yield) of 5-benzylaminosalylic acid as a white solid.: mp 173.5-174.5° C. (decompose).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750045B2
Source datasetuspto-grants-2010_07
ORD IDord-1dcc26cd1ba54cb780887f80bcf05b33
Source noteuspto-grants-2010_07