HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623016Generated: October 31, 2026
Trifluoroacetic acid → 4-(4-(Heptyloxy)phenyl)piperidine
https://huagongshe.com/reaction/1623016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Tert-butyl 4-(4-(heptyloxy)phenyl)-4-hydroxypiperidine-1-carboxylate | HCID 86689685 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-(Heptyloxy)phenyl)piperidine | HCID 86689686 | 60.9% |
Reaction Steps
To a stirring solution of tert-butyl 4-(4-(heptyloxy)phenyl)-4-hydroxypiperidine-1-carboxylate (388 mg, 0.99 mmol) and triethylsilane (791 μl, 4.95 mmol) in DCM (2 mL) cooled to −30° C. was slowly added 2,2,2-trifluoroacetic acid (379 μl, 4.95 mmol) in a drop-wise fashion. The reaction mixture was allowed to warm slowly and stirring continued for 16 h. The reaction mixture was poured onto ice-water/NaOH (50 mL/5 mL, 2 M) and extracted with DCM (3×20 mL). The combined organic extracts were washed successively with water (50 mL) and NaHCO3 (20 mL), dried over MgSO4 and evaporated to afford 166 mg (58%) of 4-(4-(heptyloxy)phenyl)piperidine INT-19 as a white, waxy solid. LCMS-ESI (m/z) calculated for C18H29NO: 275.4; found 276.0 [M+H]+, tR=2.88 min. (Method 11).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778923B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-4bc3d9021ed24138bcded300e4f886e9 |
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| Source note | uspto-grants-2014_07 |
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