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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497356Generated: October 27, 2026

tert-butyl 4-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylate → 4-(5-chloro-[1H]-indol-3-yl)-piperidine

https://huagongshe.com/reaction/497356

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylateHCID 12072033—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
Product4-(5-chloro-[1H]-indol-3-yl)-piperidineHCID 12831375146.2%

Reaction Steps

4-(5-Chloro-1H-indol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (3.4 g, 10.2 mmol) was set stirring in 1:1 TFA/CH2Cl2. After 45 min the mixture was evaporated and the golden oil brought up in Et2O. A solid formed and was filtered, washed with Et2O and air dried to give 3.5 g (97%) of a white solid as a TFA salt. MS (electrospray): exact mass calculated for C12H15ClN2, 234.09; m/z found, 235.1 [M++H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949540B2
Source datasetuspto-grants-2005_09
ORD IDord-ec7b4605b11f4d08bee855488c8461c8
Source noteuspto-grants-2005_09