Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 5-(2-Chloroethoxy)-1-benzothiophene

Benzo[b]thiophen-5-ol (0.5 g, 3.3 mmol, prepared in an analogous manner to a literature preparation: Synthetic Communications 21(7), 959-964, 1991) was dissolved in anhydrous acetonitrile (10 mL) was treated with chloroethyltosylate (0.94 g, 3.99 mmol) and cesium carbonate (2.15 g, 6.6 mmol). The mixture was stirred at reflux under nitrogen. After 2 h, the reaction was allowed to cool down to room temperature. The volatiles were removed in vacuo and the residue dissolved in ethyl acetate. The organic solution was washed with a saturated aqueous solution of sodium bicarbonate, water and brine. The ethyl acetate layer was then dried with sodium sulfate and purified by flash chromatography using a gradient of 5 to 25% of ethyl acetate in hexanes to obtain a white solid. Yield=0.676 g.

1. temperatureat reflux under nitrogen
2. customThe volatiles were removed in vacuo
3. dissolutionthe residue dissolved in ethyl acetate
4. washThe organic solution was washed with a saturated aqueous solution of sodium bicarbonate, water and brine
5. dry with materialThe ethyl acetate layer was then dried with sodium sulfate
6. custompurified by flash chromatography
7. customto obtain a white solid

ORD record

ord-0dacb8e7f0c6466ebaf36a8988865c13

Source dataset

uspto-grants-2010_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07858785B2