HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709586Generated: October 29, 2026
Methyl iodide → Dimethyl 3-hydroxyphthalate
https://huagongshe.com/reaction/709586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3-Hydroxyphthalic anhydride | HCID 96580 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 3-hydroxyphthalate | HCID 12223651 | 77% |
Reaction Steps
A stirred mixture of 3-hydroxyphthalic anhydride (20.5 g, 125 mmol) in methanol (100 mL) was heated to reflux for three hours. The solvent was evaporated in vacuo, and the residue was suspended in sodium bicarbonate (29.4 g, 350 mmol) in DMF (250 mL), followed by addition of iodomethane (19 mL, 300 mmol) and heating at 55° C. for four hours. The mixture was cooled to room temperature, solvent evaporated in vacuo, and the residue was partitioned between water (200 mL) and ethyl acetate (200 mL). The organic layer was washed with water (2×200 mL), dried, concentrated in vauco, and then purified by flash column chromatography (Silica Gel, EtOAc/Hexane, 0% gradient to 100% 30 min) to give 3-hydroxyphthalic acid dimethyl ester (20.2 g, 77% yield). The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181216B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-25bf5785d1d6488693f3410c67ad2249 |
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| Source note | uspto-grants-2015_11 |
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