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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592076Generated: October 30, 2026

Trifluoroacetic acid → 3-(2-Oxo-2-(piperazin-1-yl)ethoxy)benzaldehyde

https://huagongshe.com/reaction/592076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-Butyl 4-(2-(3-formylphenoxy)acetyl)piperazine-1-carboxylateHCID 89725867—
SolventDichloromethaneHCID 6344—
Product3-(2-Oxo-2-(piperazin-1-yl)ethoxy)benzaldehydeHCID 89726202—

Reaction Steps

tert-butyl 4-(2-(3-formylphenoxy)acetyl)piperazine-1-carboxylate (49)/(5.55 mmol) was taken in DCM and cooled to 0° C. when TFA (5 ml) was added drop wise and then stirred at rt for 16 h when TLC confirmed completion of reaction. The reaction mixture was concentrated and neutralized with satd NaHCO3 solution followed by extraction with DCM. The combined organic extracts was dried, concentrated and used directly for the next step (86%). LCMS: 98.12% (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-c18d9be70abe4cc89c3413b3ee5ddc00
Source noteuspto-grants-2016_01