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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567376Generated: October 25, 2026

Water → 1H-Indole, 4-methoxy-1-(phenylmethyl)-

https://huagongshe.com/reaction/567376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant4-Methoxy-1H-indoleHCID 138363—
SolventDimethylformamideHCID 6228—
Product1H-Indole, 4-methoxy-1-(phenylmethyl)-HCID 10728583—

Reaction Steps

NaH (7.7 g, 191.7 mmol) was added portionwise to a 0° C. solution of 4-methoxyindole (21.7 g, 147 mmol) in 750 mL of anhydrous DMF. After 15 min, the slurry was treated with benzyl bromide (17.5 mL, 147 mmol). The reaction mixture was allowed to warm to ambient temperature and stir overnight. The reaction mixture was poured into 1 L of H2O. The layers were separated, and the aqueous phase was extracted with EtOAc (2×200 mL). The combined organic layers were washed with H2O (4×500 mL), dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2; hexanes) to give 32.9 g (138.6 mmol; 94%) of the title compound as a white solid. Electrospray MS 238 (M+1);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-36b4eb5564264aae8defa89d43121e36
Source noteuspto-grants-2001_01