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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035196Generated: October 30, 2026

Trifluoroacetic acid → 1-(4-(Azetidin-3-yloxy)-2-fluorobenzyl)-4-methylpiperazine

https://huagongshe.com/reaction/1035196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 3-(3-fluoro-4-((4-methylpiperazin-1-yl)methyl)phenoxy)azetidine-1-carboxylateHCID 58043154—
SolventDichloromethaneHCID 6344—
Product1-(4-(Azetidin-3-yloxy)-2-fluorobenzyl)-4-methylpiperazineHCID 6665348032%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 29C (0.9 g, 2.4 mmol) in DCM (20 mL) was treated with TFA (10 g, 88 mmol) and stirred at 0° C. for 4 h. The reaction mixture was concentrated and the residue was dissolved in aqueous NaHCO3 (sat.). The mixture was extracted three times with DCM and the organic solutions were filtered through a phase separator. The solvent was removed by evaporation. There was obtained 0.21 g (32%) of 29D as a colorless oil. 1H NMR (500 MHz, CDCl3): δ 2.28 (s, 3H), 2.28-2.68 (bm, 8H), 3.52 (s, 2H), 3.69-3.85 (m, 2H), 3.85-4.02 (m, 2H), 4.88-5.03 (m, 1H), 6.36-6.58 (m, 2H), 7.15-7.27 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546375B2
Source datasetuspto-grants-2013_10
ORD IDord-b637d2ba530f4ba58e53b53bfa8073e8
Source noteuspto-grants-2013_10