HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529090Generated: October 30, 2026
CID 16711988 → Tert-butyl 5-fluorospiro[indoline-3,3'-piperidine]-1'-carboxylate
https://huagongshe.com/reaction/529090
Participants
| Role | Name | HCID | Charge |
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| Reactant | CID 16711988 | HCID 16711988 | — |
| Reactant | Tert-butyl 5-fluoro-2-oxospiro[indoline-3,3'-piperidine]-1'-carboxylate | HCID 23500714 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 5-fluorospiro[indoline-3,3'-piperidine]-1'-carboxylate | HCID 69811766 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346805B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-f1feb520ab654c31bffa9140c7af3f58 |
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| Source note | uspto-grants-2016_05 |
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