Water → 2-Hydroxymethyl-8-methoxy-1,4-benzodioxan

Temperature

45 °C

A mixture of 5.52 g of 8-hydroxy-2-hydroxymethyl-1,4-benzodioxan (prepared as described in EP 210581), 4.2 g 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.

1. stirringstirring
2. waitAfter 8 hours
3. stirringthe reaction mixture was stirred at 45° C. for 6 hours
4. temperatureThereafter, the mixture was cooled to room temperature
5. extractionextracted with ethyl acetate
6. washThe organic layer was washed with 6N aqueous sodium hydroxide solution, water
7. customdried on sodium sulfate
8. customEvaporation of the organic layer to dryness in vacuo

ORD record

ord-8f8a3091a7a3426ba9191b01613e1399

Source dataset

uspto-grants-1995_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05474994