HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561187Generated: October 26, 2026
Triphenylphosphine → Tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate
https://huagongshe.com/reaction/561187
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Trifluoromethylphenol | HCID 67958 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate | HCID 46941590 | — |
Reaction Steps
To a solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (25 g, 124 mmol), 2-hydroxy-benzotrifluoride (22 g, 136 mmol) and triphenylphosphine (39 g, 149 mmol) in THF was added diethyl azodicarboxylate (23.5 mL, 149 mmol) dropwise at 0° C. The mixture was then warmed to room temperature and stirred for 14 h. The mixture was concentrated and diluted with Et2O, washed with 1 N NaOH and water and then dried over Na2SO4. The mixture was concentrated and diluted with Et2O/hexanes (35:65). The precipitated phosphine oxide was filtered and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (eluting with 35% Et2O/hexanes) to give tert-butyl 4-[2-(trifluoromethyl)phenoxy]-piperidine-1-carboxylate as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063224B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-22d4009b29a4441e9cef57dbc9ec5a72 |
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| Source note | uspto-grants-2011_11 |
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