HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300560Generated: October 29, 2026
Methyl iodide → Methyl 2-(3-formylphenoxy)acetate
https://huagongshe.com/reaction/2300560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3-Formylphenoxy)acetic acid | HCID 601895 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(3-formylphenoxy)acetate | HCID 1494380 | 87.5% |
Reaction Steps
A mixture of (3-formyl-phenoxy)-acetic acid (3.6 g, 20.0 mmol), potassium carbonate (3.30 g, 23.9 mmol) and methyl iodide (1.86 g, 30.0 mmol) in 25 mL DMF was heated to 110° C. for 2 hours and was stirred at room temperature for 16 h. The mixture was diluted with water and the aqueous solution was extracted with EtOAc. The organic solution was washed with water, dried over MgSO4, filtered and concentrated in vacuo. The product was purified via silica gel chromatography (4:1 hexanes:EtOAc) to afford the title compound as a pale yellow oil (3.4 g). 1H NMR (400 MHz, CDCl3) δ 9.94 (s, 1H), 7.48 (m, 2H), 7.33 (s, 1H), 7.23 (m, 1H), 4.68 (s, 2H), 3.79 (s, 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498172B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-08133270ab5c446f96a8112a729a075b |
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| Source note | uspto-grants-2002_12 |
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