HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361475Generated: October 30, 2026
Boron tribromide → 1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]piperazine
https://huagongshe.com/reaction/1361475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Benzyl 4-(4-(2-fluorophenyl)thiazol-2-yl)piperazine-1-carboxylate | HCID 15984569 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]piperazine | HCID 58182733 | — |
Reaction Steps
To a solution of benzyl 4-(4-(2-fluorophenyl)thiazol-2-yl)piperazine-1-carboxylate (0.85 g, 2.1 mmol) in CH2Cl2 (2 μL) cooled to −50° C. was added boron tribromide (1 M in CH2Cl2, 8.6 mL, 8.6 mmol). The reaction was stirred at −50° C. for 20 min and then carefully quenched with saturated aqueous NaHCO3. The mixture was extracted with CH2Cl2, and the combined extracts were washed with water, dried over Na2SO4, and concentrated under reduced pressure to yield 1-(4-(2-fluorophenyl)thiazol-2-yl)piperazine. LC/MS: m/z 264.1 (M+H)+ at 2.04 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880008B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-3f60637d4abd47f99a648cf971372941 |
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| Source note | uspto-grants-2011_02 |
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