HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855673Generated: October 28, 2026
Potassium Iodide → 3-Methoxy-4-(3-morpholinopropoxy)benzoic acid
https://huagongshe.com/reaction/855673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Vanillic Acid | HCID 8468 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(3-Chloropropyl)morpholine | HCID 95834 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-4-(3-morpholinopropoxy)benzoic acid | HCID 21699284 | 109.3% |
Reaction Steps
A mixture of 4-hydroxy-3-methoxybenzoic acid (4.5 g, 26.8 mmol), 3-morpholinopropyl chloride (9.5 g, 58.0 mmol), (prepared according to J. Am. Chem. Soc. 1945, 67, 736), potassium carbonate (8.0 g, 58 mmol), potassium iodide (1.0 g, 0.22 mmol) and DMF (80 ml) was stirred and heated at 100° C. for 3 hours. The solid was removed by filtration and the volatiles were removed by evaporation. The residue was dissolved in ethanol (50 ml), 2M sodium hydroxide (50 ml) was added and the mixture heated at 90° C. for 2 hours. After partial evaporation, the mixture was acidified with concentrated hydrochloric acid, washed with ether and then subjected to purification on a Diaion (trade mark of Mitsubishi) HP20SS resin column, eluting with water and then with a gradient of methanol (0 to 25%) in hydrochloric acid (pH2). Partial evaporation of the solvents and lyophilisation gave 3-methoxy-4-(3-morpholinopropoxy)benzoic acid (8.65 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262201B1 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-41d29b83a838441eb3a18c607976795d |
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| Source note | uspto-grants-2007_08 |
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