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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 3-(2-methyl-4-((4-methylpiperazin-1-yl)methyl)phenoxy)azetidine-1-carboxylate | HCID 58043145 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-(Azetidin-3-yloxy)-3-methylbenzyl)-4-methylpiperazine | HCID 67016551 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546375B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0c03900dfaae403aa085f24014b052d0 |
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| Source note | uspto-grants-2013_10 |
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