HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509821Generated: October 28, 2026
5-Aminosalicylic Acid → 5-benzylaminosalicylic acid
https://huagongshe.com/reaction/1509821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminosalicylic Acid | HCID 4075 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-benzylaminosalicylic acid | HCID 9899588 | 113.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211878B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-4826e601ad6441588a9fa3cbda3882ff |
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| Source note | uspto-grants-2012_07 |
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