Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-indol-4-ol | HCID 75421 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Ethoxy-1H-indole | HCID 15370717 | — |
Reaction Steps
An oven dried two neck flask was charged with 5 ml DMF and NaH (66 mg, 60% in oil, 1.65 mmol). The mixture was cooled down to 0° C., followed by dropwise addition of 4-hydroxy indole (200 mg, 1.5 mmol) in 5 ml DMF over 10 second. After stirring for 30 min under N2, bromoethane in 2 ml DMF was added dropwise, and the reaction was allowed to warm to rt. with continued stirring for 2 hr. Removal of the solvent in vacuo, followed by aqueous work up afforded crude 4-ethoxyindole which was purified by prep. HPLC to afford 201 mg (83%) of pure 4-ethxyindole; HPLC retention time, 1.190 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469006B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-e0fd77c0b1b44a78abab0ce011b61f46 |
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| Source note | uspto-grants-2002_10 |
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