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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 6-fluoro-2,3-dihydro-1H-indole | HCID 260400 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238658B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b2d5a6cb376e42f7ab91332e28db0afd |
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| Source note | uspto-grants-2016_01 |
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