HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876449Generated: October 28, 2026
Aluminium lithium hydride → tert-Butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/876449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl N-Boc-4-fluoropiperidine-4-carboxylate | HCID 21306965 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate | HCID 22248400 | 105.8% |
Reaction Steps
To a 0° C. solution of 1-tert-butyl 4-ethyl 4-fluoropiperidine-1,4-dicarboxylate (3.0 g, 10.90 mmol) in 55 mL THF was added 1M lithium aluminum hydride in THF (21.79 mL, 21.79 mmol). The reaction mixture was stirred at 0° C. for 3.5 hours, after which it was carefully quenched by the addition of 1:1 Na2SO4-10H2O:Celite, diluted with THF, warmed to ambient temperature, and stirred vigorously for 2 hours. The slurry was vacuum filtered through GF/F paper on a Buchner funnel, rinsed with THF, and the filtrate was concentrated in vacuo to give the title compound (2.69 g) as a clear colorless oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987251B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0a5e1c7be3ed4020aba82f8b5f48384a |
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| Source note | uspto-grants-2015_03 |
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