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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantBenzyl 4-(4-(2-fluorophenyl)thiazol-2-yl)piperazine-1-carboxylateHCID 15984569—
SolventDichloromethaneHCID 6344—
Product1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]piperazineHCID 58182733—

Reaction Conditions

Temperature-50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880008B2
Source datasetuspto-grants-2011_02
ORD IDord-3f60637d4abd47f99a648cf971372941
Source noteuspto-grants-2011_02