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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190028Generated: November 1, 2026

CID 16711988 → Tert-butyl 5-fluorospiro[indoline-3,3'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/2190028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 16711988HCID 16711988—
ReactantTert-butyl 5-fluoro-2-oxospiro[indoline-3,3'-piperidine]-1'-carboxylateHCID 23500714—
SolventTolueneHCID 1140—
ProductTert-butyl 5-fluorospiro[indoline-3,3'-piperidine]-1'-carboxylateHCID 6981176624%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of tert-butyl 5-fluoro-2-oxospiro[indoline-3,3′-piperidine]-1′-carboxylate (0.80 g, 2.5 mmol) in toluene (20 mL) was added dropwise a solution of sodium bis(2-methoxyethoxy) aluminium hybrid (Red-Al) in toluene (65% w/w, 1.1 mL, 3.5 mmol) at about 70° C. under N2. The reaction mixture was stirred at about 75° C. for 3 h. After cooling, the reaction mixture was quenched with EtOAc and concentrated in vacuo. The residue was diluted with EtOAc, washed with water and brine, dried and concentrated. The residue was purified by column chromatography (hexane:EtOAc, 3:1) to give tert-butyl 5-fluorospiro[indoline-3,3′-piperidine]-1′-carboxylate (0.18 g, 24%) as an oil. LCMS (APCI+) m/z 307 [M+H]+; Rt=3.66 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324221B2
Source datasetuspto-grants-2012_12
ORD IDord-be74702628c0416ba4fed80ff87e9045
Source noteuspto-grants-2012_12