HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625385Generated: October 25, 2026
Potassium Iodide → 3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acid
https://huagongshe.com/reaction/625385
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Ethanediamine, N1,N1-diethyl-N2-methyl- | HCID 66034 | — |
| Reactant | 3-(Bromomethyl)benzoic acid | HCID 245650 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acid | HCID 66586839 | 48.8% |
Reaction Steps
Into a 1000-mL round bottom flask, was placed a solution of N1,N1-diethyl-N2-methylethane-1,2-diamine (9.1 g, 63.00 mmol, 1.50 equiv, 90%) in N,N-dimethylformamide (500 mL), 3-(bromomethyl)benzoic acid (10 g, 46.51 mmol, 1.00 equiv), potassium carbonate (7.8 g, 56.12 mmol, 1.20 equiv), and potassium iodide (1.55 g, 9.34 mmol, 0.20 equiv). The resulting solution was stirred for 2 h at 90° C. in an oil bath. The solids were filtered out. The resulting mixture was concentrated under vacuum. The crude product (10 g) was purified by reverse phase HPLC eluting with 0.05% TFA in a water/CH3CN gradient. The product was obtained as 6 g (46%) of a white solid. 1H-NMR (300 MHz, CDCl3, ppm): δ 8.01 (m, 1H), 7.89-7.87 (m, 1H), 7.28-7.22 (m, 2H), 3.99 (s, 2H), 2.97-2.72 (m, 8H), 2.28 (s, 3H), 1.13-1.01 (m, 6H). MS (ES, m/z): 265 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301951B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-caf790e52b57421fbc5fcb5407053606 |
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| Source note | uspto-grants-2016_04 |
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