Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379737Generated: November 1, 2026

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

https://huagongshe.com/reaction/1379737

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 numberUS05672618
Source datasetuspto-grants-1997_09
ORD IDord-1060149b251a47b7af8936d4ff3497c2
Source noteuspto-grants-1997_09