HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82920Generated: October 27, 2026
4-Fluorophenol → Tert-butyl 3-[(4-fluorophenoxy)methyl]piperidine-1-carboxylate
https://huagongshe.com/reaction/82920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate | HCID 2763851 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-[(4-fluorophenoxy)methyl]piperidine-1-carboxylate | HCID 67154710 | 42% |
Reaction Steps
4-Fluorophenol (520 mg, 4.64 mmol) and triphenylphosphine (1.22 g, 4.64 mmol) were added to a solution of N-boc-piperidine-3-methanol (500 mg, 2.32 mmol) in anhydrous THF (12 mL) under nitrogen. The reaction mixture was cooled to 0° C. and DEAD (673 μL, 3.71 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure then diluted with dichloromethane and filtered. The filtrate was washed three times with NaOH 0.2N, dried over Na2SO4 and concentrated. The residue was purified on column chromatography (eluent: pentane/EtOAc 95/5) to give the title compound (300 mg, 42%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846711B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-752a4d634f02451ba8db3d2b3d1e97f2 |
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| Source note | uspto-grants-2014_09 |
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