HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081470Generated: October 25, 2026
1-Benzylpiperazine → 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine
https://huagongshe.com/reaction/2081470
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride | HCID 15053367 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[3-(4-Fluorophenoxy)-1-azetidinylcarbonyl]-4-(phenylmethyl)piperazine | HCID 15053405 | 108.3% |
Reaction Steps
A stirred solution of 6.9 g (0.03 mole) of 3-(4-fluorophenoxy)-1-azetidinecarbonyl chloride in 60 ml of methylene chloride was treated with 10.8 g (0.06 mole) of 1-benzylpiperazine, added dropwise. After stirring for 18 hr, the reaction mixture was diluted with 200 ml of water and stirred for an additional 1 hr. The methylene chloride portion was separated and the aqueous portion was extracted with 2×25 ml of methylene chloride. The methylene chloride portions were combined, dried and concentrated in vacuo, yielding 12 g of oil residue. This oil solidified when triturated with ligroin and was recrystallized from benzene/ligroin to yield 10.1 (91%) of tan crystals. A 500 mg portion was recrystallized from benzene/ligroin to yield 250 mg of fine white crystals, m.p. 109°-111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05183902 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-4de2d497d3874acd9bd0e1c65deb41a2 |
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| Source note | uspto-grants-1993_02 |
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