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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580898Generated: October 26, 2026

2-Bromoethanol → 4-(1H-indol-1-yl)-1-piperidineethanol

https://huagongshe.com/reaction/580898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Piperidin-4-yl)-1H-indoleHCID 14090755—
SolventEthanolHCID 702—
Product4-(1H-indol-1-yl)-1-piperidineethanolHCID 5384824865.6%

Reaction Steps

A mixture of 2-bromoethanol (3.75 g), 1-(4-piperidinyl)-1H-indole (5 g) and sodium hydrogen carbonate (4.2 g) in ethanol (100 ml) was stirred and refluxed overnight. The solvent was evaporated. The residue was stirred in water and this mixture was extracted with CH2Cl2. The separated organic layer was dried over MgSO4, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH 95/5). The pure fractions were collected and the solvent was evaporated. The residue was stirred in DIPE and the solvent was evaporated, yielding 4 g (64%) of 4-(1H-indol-1-yl)-1-piperidineethanol (intermediate 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919788
Source datasetuspto-grants-1999_07
ORD IDord-fe4e4315e4ad44858b4b7ae5bc44681b
Source noteuspto-grants-1999_07