HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378869Generated: October 26, 2026
Water → 2-(Piperazin-1-yl)-1,3-benzoxazole
https://huagongshe.com/reaction/378869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Piperazin-1-yl)-1,3-benzoxazole | HCID 647818 | — |
Reaction Steps
Anhydrous piperazine (5.6 g) was dissolved in methylene chloride (100 ml) to which was subsequently added triethylamine (4.5 ml). With cooling in an ice bath, to this was added dropwise 2-chlorobenzoxazole (3.7 ml) in small portions, followed by 45 minutes of stirring. The reaction solution was mixed with water, extracted with methylene chloride and then washed with saturated sodium bicarbonate aqueous solution and saturated brine in that order. The organic layer was dried with magnesium sulfate and the solvent was evaporated under a reduced pressure. Thereafter, the thus obtained mixture was purified by a silica gel column chromatography (methanol) to obtain the title compound 2-(1-piperazinyl)benzoxazole (4.751 g) in the form of yellow crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297246B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-ff7350910e244f25bb4f59ef1e133268 |
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| Source note | uspto-grants-2001_10 |
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