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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677258Generated: November 1, 2026

Toluene → 5-benzyloxy-6-isopropyl-1,3-dimethyl-1H-indole

https://huagongshe.com/reaction/1677258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant5-benzyloxy-6-isopropyl-3-methyl-1H-indoleHCID 59598603—
CatalystBenzyltributylammonium chlorideHCID 159952—
SolventWaterHCID 962—
Product5-benzyloxy-6-isopropyl-1,3-dimethyl-1H-indoleHCID 59598742—

Reaction Conditions

Temperature90 °C

Reaction Steps

5-Benzyloxy-6-isopropyl-3-methyl-1H-indole (0.320 g, 1.15 mmol), KOH (0.264 g, 4.7 mmol), benzyl tributylammonium chloride (0.071 g, 0.230 mmol), and methyl iodide (0.107 mL, 1.72 mmol) were added to 3 mL of toluene. The resulting mixture was stirred for 4 hours at 90° C., cooled to room temperature, poured into water, and extracted with ethyl acetate 2 times. The combined organic layers were washed with water, dried (MgSO4), and evaporated in vacuo to provide a crude oil that was was purified with flash chromatography (ethyl acetate/hexanes 1/9); yield 270 mg of 5-benzyloxy-6-isopropyl-1,3-dimethyl-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-0363796cdb5447f0bcfe6608b70f4f94
Source noteuspto-grants-2011_08