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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279385Generated: October 31, 2026

Sodium Hydroxide → 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole

https://huagongshe.com/reaction/1279385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indoleHCID 18427956—
SolventEthanolHCID 702—
Product5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indoleHCID 1064107380.4%

Reaction Steps

A mixture of 1-benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole (1.49 g, 3.1 mmol) is stirred in EtOH (200 mL) and 50% NaOH (1 mL) at room temperature for 3 days. Most of the EtOH is evaporated and the residue diluted with water (200 mL). The precipitate is filtered off and washed copiously with water. The precipitate is recrystallized from hot EtOH to give the title compound as an off-white solid (854 mg): mp 165-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448270B1
Source datasetuspto-grants-2002_09
ORD IDord-108c3faaac79487d9efe13dbf5711002
Source noteuspto-grants-2002_09