HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55924Generated: October 25, 2026
5-Methoxyindole → 5-methoxy-3-(1-naphthoyl)-1H-indole
https://huagongshe.com/reaction/55924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Methoxyindole | HCID 13872 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Naphthalenecarbonyl chloride | HCID 70146 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-methoxy-3-(1-naphthoyl)-1H-indole | HCID 68159287 | 75% |
Reaction Steps
To a cooled solution at 0° C. of 5-methoxy-1H-indole 3 (7.4 g, 50 mmol) in diethyl ether (150 ml) under nitrogen was added dropwise a solution of methylmagnesium bromide (3M) in diethyl ether (17.5 ml) and the mixture was stirred for 2 h at room temperature. The solution was then cooled at 0° C. and to this solution was added a solution of 1-naphthoylchloride (9.5 g, 50 mmol) in diethyl ether (100 ml) dropwise over a period of 15 min. After the addition was completed the solution was warmed up at room temperature and stirred for 2 h followed by slow addition of saturated ammonium chloride solution (375 ml) and stirred overnight. The white solid formed was filtered, washed by ether and dried under high vacuum to give 5-methoxy-3-(1-naphthoyl)-1H-indole 4 (11.3 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434687B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-fe93391650c3489caaf5e02e57804c70 |
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| Source note | uspto-grants-2016_09 |
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