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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456965Generated: October 30, 2026

Sodium hydride → 4-Cyclopropylmethoxyindole

https://huagongshe.com/reaction/1456965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1H-indol-4-olHCID 75421—
ReactantBromomethylcyclopropaneHCID 81503—
SolventDimethylformamideHCID 6228—
Product4-CyclopropylmethoxyindoleHCID 2126829464%

Reaction Steps

A solution of 5.00 gm (37.6 mmol) 4-hydroxyindole in dimethylformamide was added dropwise over 30 minutes to a solution of 1.65 gm (41.3 mMol) sodium hydride (60% suspension in mineral oil) in 25 mL dimethylformamide at 0° C. The resulting black solution was stirred at room temperature for 2 hours and then a solution of 3.6 mL (37.6 mMol) cyclopropylmethyl bromide in 10 mL dimethylformamide was added dropwise. The resulting mixture was stirred for 1.5 hours at room temperature. The reaction mixture was then quenched by the addition of 100 mL water and the resulting mixture extracted well with ethyl acetate. The organic phases were combined, washed sequentially with water and saturated aqueous sodium chloride, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 10% ethyl acetate in hexane. Fractions shown to contain product were combined and concentrated under reduced pressure to provide 4.48 gm (64%) of the title compound as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846982
Source datasetuspto-grants-1998_12
ORD IDord-e2a418238dd8469d8146dc1e9a5eaba1
Source noteuspto-grants-1998_12