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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-MethoxyindoleHCID 13872—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Naphthalenecarbonyl chlorideHCID 70146—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product5-methoxy-3-(1-naphthoyl)-1H-indoleHCID 6815928775%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434687B2
Source datasetuspto-grants-2016_09
ORD IDord-fe93391650c3489caaf5e02e57804c70
Source noteuspto-grants-2016_09