HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452342Generated: November 1, 2026
Water → 2-Hydroxymethyl-8-methoxy-1,4-benzodioxan
https://huagongshe.com/reaction/1452342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 8-Hydroxy-1,4-benzodioxan-2-ylmethanol | HCID 14349188 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Hydroxymethyl-8-methoxy-1,4-benzodioxan | HCID 10488108 | 90% |
Reaction Steps
A mixture of 5.52 g of 8-hydroxy-2-hydroxymethyl-1,4-benzodioxan (prepared as described in EP 210581), 4.2g of anhydrous potassium carbonate and 2.06 ml of methyl iodide in 75 ml of anhydrous dimethylformamide was stirred at 45° C. for 8 hours. Methyl iodide (1 ml) was added to the mixture and stirring continued at the same temperature. After 8 hours, 1 ml of methyl iodide and 2.1 g of potassium carbonate were further added, and the reaction mixture was stirred at 45° C. for 6 hours. Thereafter, the mixture was cooled to room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with 6N aqueous sodium hydroxide solution, water, then dried on sodium sulfate. Evaporation of the organic layer to dryness in vacuo afforded 5.35 g of 2-hydroxymethyl-8-methoxy-1,4-benzodioxan, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605896 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-cb76fbd2c59446ce913038f001200505 |
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| Source note | uspto-grants-1997_02 |
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