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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41063Generated: October 26, 2026

Potassium Carbonate → 5-Cyclopropylmethoxy-1H-indol

https://huagongshe.com/reaction/41063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-HydroxyindoleHCID 16054—
ReactantBromomethylcyclopropaneHCID 81503—
SolventAcetoneHCID 180—
Product5-Cyclopropylmethoxy-1H-indolHCID 57436983—

Reaction Steps

To a solution of 7.3 g 5-hydroxy-indole in 130 ml of dry acetone are added 10.5 ml bromomethyl cyclopropane and 22.7 g anhydrous potassium carbonate. The mixture is heated to reflux for 24 h and an additional amount of 5 ml bromomethyl cyclopropane are added. The mixture is heated to reflux for additional 4 days. The mixture is filtered and the solvent is removed under reduced pressure. The residue is dissolved in dichloro methane and washed with an aqueous solution of hydrochloric acid (2 M), 10% aq. NaHCO3 and water. The organic layer is dried and the solvent is removed under reduced pressure. After purification by column chromatography (silica gel; toluene, acetone 95:5), 9.62 g, 94%) of the title compound are obtained as an oil. 1H-NMR (CDCl3): 0.36 (m, 2H, cyclopropyl CH2), 0.64 (m, 2H, cyclopropyl CH2), 1.30 (m, 1H, cyclopropyl CH), 3.83 (d, 2H, J=7.0 Hz, CH2O), 6.45 (s, 1H, aromatic), 6.90 (dd, 1H, aromatic), 7.09-7.27 (m, 3H, aromatic), 8.05 (bs, 1H, NH). 13C-NMR (CDCl3): 3.1 (2 cyclopropyl CH2), 10.4 (cyclopropyl CH), 74.2 (CH2O), 101.2, 101.6, 104.0, 104.6, 149.8 (aromatic)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530493B2
Source datasetuspto-grants-2013_09
ORD IDord-6920e4434f3d4db69bd1d676b22b48e8
Source noteuspto-grants-2013_09