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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515273Generated: October 25, 2026

Trifluoroacetic acid → 4-(2-Bromo-4-nitrophenoxy)piperidine

https://huagongshe.com/reaction/515273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylateHCID 18542613—
SolventDichloromethaneHCID 6344—
Product4-(2-Bromo-4-nitrophenoxy)piperidineHCID 6234763989.8%

Reaction Steps

tert-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate (12.21 mmol, 4.9 g) was dissolved in dichloromethane (40 mL) and trifluoroacetic acid (73.3 mmol, 8.35 g) added. The mixture was stirred at room temperature for 3 hours before concentrating under reduced pressure. The resulting residue was dissolved in dichloromethane (150 mL) and washed with a saturated solution of sodium bicarbonate (3×50 mL). The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford the title compound (3.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108939B2
Source datasetuspto-grants-2015_08
ORD IDord-157047b09cd64502ad69424ba9779bf6
Source noteuspto-grants-2015_08