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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736966Generated: October 25, 2026

3-(6-Methoxy-cyclohex-1-enyl)-1H-indole → 3-(2-Methoxy-cyclohexyl)-1H-indole

https://huagongshe.com/reaction/736966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(6-Methoxy-cyclohex-1-enyl)-1H-indoleHCID 58975073—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-(2-Methoxy-cyclohexyl)-1H-indoleHCID 5897509463%

Reaction Steps

Treat 3-(6-methoxy-cyclohex-1-enyl)-1H-indole (200 mg, 0.879 mmol) with 10% Pd/C (40 mg) in EtOAc under atmospheric hydrogenation conditions for 1.5 hours. Filter resulting solution over Celite to remove catalyst. Concentrate crude on rotovap and purify on silica gel chromatography to give 3-(2-Methoxy-cyclohexyl)-1H-indole (127 mg, 63% yield). Mass Spectrum (m/e): 230.03 (MH+), 228.14 (M−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595339B2
Source datasetuspto-grants-2009_09
ORD IDord-683d20d846bf496d957543d5f33f089d
Source noteuspto-grants-2009_09