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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591345Generated: October 26, 2026

Sodium Carbonate → Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/591345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant6-fluoro-2,3-dihydro-1H-indoleHCID 260400—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylateHCID 89613009—

Reaction Steps

To a solution of 6-fluoroindoline (9.36 g, 68 mmol) in CH2Cl2 (100 mL) was added 1-Boc-4-piperidone (13.6 g, 68 mmol). The resulting mixture was stirred at room temperature for 1 h and NaBH(OAc)3 (18 g, 85 mmol, 1.25 equiv) was added. The resulting mixture was stirred at room temperature for 24 h and was then poured slowly to a vigorously stirred Na2CO3(aq). After 30 min stirring, the layers were separated. The aqueous layer was extracted with CH2Cl2 (100 mL). The combined organic layer was washed with brine (100 mL), dried (Na2SO4), and filtered. The solvent was removed by roto-evaporator, Et2O (10 mL) and then hexane (150 mL) were added to the resulting residue. The mixture was allowed to stand, resulting in the formation of a white solid, which was collected and washed with 5% Et2O/hexane and then dried. This was repeated to yield three crops of tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238658B2
Source datasetuspto-grants-2016_01
ORD IDord-b2d5a6cb376e42f7ab91332e28db0afd
Source noteuspto-grants-2016_01