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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantTert-butyl 4-(4-(heptyloxy)phenyl)-4-hydroxypiperidine-1-carboxylateHCID 86689685—
SolventDichloromethaneHCID 6344—
Product4-(4-(Heptyloxy)phenyl)piperidineHCID 8668968660.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778923B2
Source datasetuspto-grants-2014_07
ORD IDord-4bc3d9021ed24138bcded300e4f886e9
Source noteuspto-grants-2014_07