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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45583Generated: October 26, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/45583

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactant5-FluoroindolineHCID 2774463—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSodium bicarbonate waterHCID 86585896—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indoleHCID 67417842—

Reaction Steps

To a solution of 5-fluoroindoline (1.0 g, 7.30 mmol) and N-Boc-4-piperidone (1.60 g, 7.50 mmol) in tetrahydrofuran (10.0 mL) was added sodium triacetoxyborohydride (1.80 g, 7.50 mmol). After stirring for 3 hours at room temperature, to the mixture were added saturated sodium bicarbonate water and ethyl acetate, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified with silica gel column (chloroform/methanol=98/2 to 90/10) to give a Boc derivative of the title compound. MS (ESI+) 321 (M++1, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541585B2
Source datasetuspto-grants-2013_09
ORD IDord-e200522c45314eee9bac792acc4c12d9
Source noteuspto-grants-2013_09