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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871131Generated: October 26, 2026

2-Bromothiazole → (3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanol

https://huagongshe.com/reaction/871131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
Reactant3-Bromo-2-fluorobenzaldehydeHCID 22019361—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanolHCID 86730392—

Reaction Steps

To a solution of 2-bromothiazole (0.088 mL, 0.985 mmol) in THF (2.99 mL) cooled to 0° C. was added isopropylmagnesium chloride (0.493 mL, 0.985 mmol). After 50 min, 3-bromo-2-fluorobenzaldehyde (0.200 g, 0.985 mmol) was added. The reaction mixture was allowed to warm to room temperature overnight. After 12 hr, the reaction was quenched with saturated aqueous NH4Cl. The reaction mixture was diluted with CH2Cl2. The layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). The organic phases were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969586B2
Source datasetuspto-grants-2015_03
ORD IDord-6212d96390894a2488576604565032f9
Source noteuspto-grants-2015_03