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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023349Generated: November 2, 2026

Trifluoroacetic acid → 1-(4-{[4-(Propan-2-yloxy)phenoxy]methyl}benzyl)piperazine

https://huagongshe.com/reaction/1023349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-(4-{[4-(propan-2-yloxy)phenoxy]methyl}benzyl)piperazine-1-carboxylateHCID 67328500—
SolventDichloromethaneHCID 6344—
Product1-(4-{[4-(Propan-2-yloxy)phenoxy]methyl}benzyl)piperazineHCID 67327697136.8%

Reaction Steps

To a solution of tert-butyl 4-(4-{[4-(propan-2-yloxy)phenoxy]methyl}benzyl)-piperazine-1-carboxylate (5.42 g) in CH2Cl2 (41 mL) was added TFA (10 mL) at room temperature, then the reaction mixture was stirred for 8 hours. The reaction mixture was basified with 5 M aqueous NaOH, and extracted with CH2Cl2. The organic layer was washed with water and saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure to afford 1-(4-{[4-(propan-2-yloxy)phenoxy]methyl}benzyl)piperazine as a colorless solid (5.73 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-dbde279ecdb747d1a9b879cd89001f0f
Source noteuspto-grants-2014_05