HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961371Generated: October 30, 2026
Methanol → 1-(4-Azetidin-3-yl-piperazin-1-yl)-2,2,2-trifluoro-ethanone
https://huagongshe.com/reaction/1961371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-[4-(1-Benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanone | HCID 59625975 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Azetidin-3-yl-piperazin-1-yl)-2,2,2-trifluoro-ethanone | HCID 59625678 | — |
Reaction Steps
To a solution of 1-[4-(1-benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanone (2.11 g, 5.23 mmol) in CH2Cl2 (60 mL) was added 1-chloroethyl chloroformate (2.0 mL, 18.35 mmol) at 0° C. under N2. The resulting mixture was stirred at 0° C. for 90 min and then methanol (4 mL) was added. The resulting mixture was refluxed for 1 h. Upon cooling, diethyl ether (50 mL) was added to the mixture. The resulting solid was collected by filtration and dried to yield the title compound, which was used in the next reaction without further purification. MS m/z (M+H+) 238.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415341B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-68586238c42340bf9a14e7599d4b9a63 |
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| Source note | uspto-grants-2013_04 |
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