HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Ethoxymethoxy-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloromethyl ethyl ether | HCID 18523 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzofuran-5-ol | HCID 11651159 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Ethoxymethoxy-benzofuran | HCID 59227450 | — |
Reaction Steps
To a stirred solution of benzofuran-5-ol (2) (257 mg, 1.92 mmol) in DMF (3 mL), NaH (81 mg, 1.92 mmol, 57% dispersion in oil) was added at 0° C. The reaction mixture was warmed to room temperature and stirred 1 hour. Chloromethyl ethyl ether (214 μL, 2.30 mmol) was then added drop wise to 0° C. and the mixture was stirred at room temperature for additional 1 hour. Water (10 mL) was added and the reaction mixture was extracted with ethyl acetate (2×50 mL). The organic extracts were washed with water, brine, dried over Na2SO4, and concentrated in vacuo. Purification of the crude product by flash column chromatography using 10% ethyl acetate in hexane afforded compound (3) (273 mg) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193363B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-bcd7bfa677e64f72a143dd07740c793d |
| Source note | uspto-grants-2012_06 |