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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856880Generated: October 25, 2026

Triethylsilane → N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine

https://huagongshe.com/reaction/1856880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant1H-Indole, 4,5,6,7-tetrafluoro-HCID 140051—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
SolventDichloromethaneHCID 6344—
ProductN-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidineHCID 1139563866%

Reaction Steps

To a solution of N-benzyloxycarbonyl-4-piperidone (20.2 g, 90.6 mmol) in methylene chloride (600 ml) at 0° C. was added trimethylsilyl trifluoromethanesulfonate (35.1 ml, 181.2 mmol) followed by the slow dropwise addition of a solution of 4,5,6,7-tetrafluoroindole (17.1 g, 90.6 mmol) in methylene chloride (300 ml) over 2.5 h. After 1.5 h, triethylsilane (57.9 ml, 362.4 mmol) was added and the reaction was allowed to warm to RT over 30 min. The reaction mixture was quenched with sat. sodium bicarbonate and the separated organic layer was dried over MgSO4 and concentrated in vacuo. The residue was partitioned between 50% acetonitrile/hexanes (1400 ml) and the separated acetonitrile layer was concentrated in vacuo. The solid residue was recrystallized from absolute EtOH to afford N-benzyloxycarbonyl-4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine (66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-6c03f3e1828a4ab295bf61ec8bc84dbb
Source noteuspto-grants-2000_11