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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275138Generated: October 30, 2026

Sodium hydride → 5-allyloxy-N-neopentylindole

https://huagongshe.com/reaction/1275138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPropane, 1-iodo-2,2-dimethyl-HCID 84953—
Reactant5-(prop-2-en-1-yloxy)-1H-indoleHCID 14239230—
SolventTetrahydrofuranHCID 8028—
Product5-allyloxy-N-neopentylindoleHCID 18672460—

Reaction Steps

To a solution of sodium hydride (60%, 254 mg, 6.35 mmol) in 15 mL tetrahydrofuran (THF) was added 5-allyloxyindole (Step A; 1.0 g, 5.77 mmol) in 5 mL THF and the mixture was stirred for 1 hour at ambient temperature. Neopentyl iodide (0.69 mL, 6.35 mmol) was added and the reaction heated to reflux for 21 hours. After cooling, the reaction was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue purified by flash chromatography on silica gel (15% ethyl acetate/hexane) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06160000
Source datasetuspto-grants-2000_12
ORD IDord-8d4340160ff04dc793a528bdda82125c
Source noteuspto-grants-2000_12