HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171618Generated: November 1, 2026
Cesium carbonate → Ethyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylate
https://huagongshe.com/reaction/2171618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | ((3-Bromo-2-fluorobenzyl)oxy)(tert-butyl)dimethylsilane | HCID 86686195 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylate | HCID 68308904 | 57.9% |
Reaction Steps
Under argon atmosphere, [(3-bromo-2-fluorobenzyl)oxy](tert-butyl)dimethylsilane (2 g) and ethyl piperidine-4-carboxylate (1.6 g) were mixed with toluene (30 ml), and Pd2(dba)3 (150 mg), BINAP (300 mg), and cesium carbonate (3.2 g) were added thereto, followed by stirring at 100° C. for 1 hour. The reaction mixture was cooled to room temperature, and EtOAc was added thereto, followed by filtration using Celite as a filtration adjuvant. The filtrate was concentrated under reduced pressure, the residue was then mixed with THF (30 ml), and a 1M TBAF/THF solution (12 ml) was added thereto, followed by stirring at room temperature for 1 hour. To the reaction mixture were added EtOAc and water, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain ethyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylate (1.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051283B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d5255b076d864d4aa2a978abae59481f |
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| Source note | uspto-grants-2015_06 |
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