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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077935Generated: October 30, 2026

4-Indol-1-yl-piperidine-1-carboxylic acid ethyl ester → 1-(1-methyl-piperidin-4-yl)-1H-indole

https://huagongshe.com/reaction/1077935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Indol-1-yl-piperidine-1-carboxylic acid ethyl esterHCID 14090749—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product1-(1-methyl-piperidin-4-yl)-1H-indoleHCID 1409074364.8%

Reaction Steps

To an ice cooled solution of 4-indol-1-yl-piperidine-1-carboxylic acid ethyl ester (50 g, 0.18 mol) in dry THF (400 mL) was added LAH in small portions (7 g, 0.18 mol). After 2 hours, the mixture was quenched by successive addition of water (7 mL) 15% of sodium hydroxide (7 mL) and water (21 mL). The reaction mixture was filtered. The filtrate was dried and evaporated. The residue crystallized on standing and was recrystallized from a small amount of di-i-propyl ether to give the title compound (25 g, 63% of theory). M.Pt.: 58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545636
Source datasetuspto-grants-1996_08
ORD IDord-6fbfa59307b64db5b2d3839a9d5a3d25
Source noteuspto-grants-1996_08