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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035175Generated: October 26, 2026

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

https://huagongshe.com/reaction/1035175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 3-(2-methyl-4-((4-methylpiperazin-1-yl)methyl)phenoxy)azetidine-1-carboxylateHCID 58043145—
SolventDichloromethaneHCID 6344—
Product1-(4-(Azetidin-3-yloxy)-3-methylbenzyl)-4-methylpiperazineHCID 6701655190%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 9B (2.18 g, 5.81 mmol) in DCM (40 mL) was treated with TFA (10 g, 88 mmol) and stirred at 0° C. for 3 h. The reaction mixture was concentrated and the residue was dissolved in aqueous NaHCO3 (sat.) and extracted several times with DCM. The organic solutions were filtered through a phase separator. The solvent was removed by evaporation and the residue was purified by column chromatography on SiO2 using 10% triethylamine and 10% MeOH in EtOAc as eluent. There was obtained 1.44 g (90%) of 9C as a colorless oil. 1H NMR (500 MHz, CDCl3): δ 2.22 (s, 3H), 2.28 (s, 3H), 2.27-2.70 (bm, 8H), 3.40 (s, 2H), 3.75-3.85 (m, 2H), 3.88-3.98 (m, 2H), 4.92-5.02 (m, 1H), 6.43 (d, 1H), 7.01 (d, 1H), 7.09 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546375B2
Source datasetuspto-grants-2013_10
ORD IDord-0c03900dfaae403aa085f24014b052d0
Source noteuspto-grants-2013_10