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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191914Generated: November 2, 2026

Sodium Iodide → tert-butyl (3S)-3-methyl-4-[6-(trifluoromethyl)-2,3-dihydro-1H-inden-1-yl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1191914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant(S)-1-Boc-3-methylpiperazineHCID 7023035—
Reactant1-Chloro-6-(trifluoromethyl)indaneHCID 59212653—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl (3S)-3-methyl-4-[6-(trifluoromethyl)-2,3-dihydro-1H-inden-1-yl]piperazine-1-carboxylateHCID 59212635—

Reaction Steps

A solution of 1-chloro-6-(trifluoromethyl)indane (1.52 g, 6.89 mmol), tert-butyl (3S)-3-methylpiperazine-1-carboxylate (2.1 g, 10 mmol), sodium iodide (3 g, 20 mmol) and triethylamine (3 g, 30 mmol) in DMF (20 mL) was stirred at 60° C. overnight. After cooling to room temperature, water was added. The resulting solution was extracted with EtOAc twice. The combined extracts were washed with water and brine, dried over MgSO4 and concentrated. Column chromatography on silica (10%-30% EtOAc in hexane) afforded two isomers. Isomer 1: 0.52 g (brown oil). MS calculated for C20H27F3N2O2: (M+H)+ 385. found 385.2. Isomer 2: 0.41 g (brown oil). MS: (M+H)+ 385.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680104B2
Source datasetuspto-grants-2014_03
ORD IDord-91c9c8eba6ef4407a195b2efa27aac61
Source noteuspto-grants-2014_03