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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182675Generated: November 2, 2026

Tetrahydrofuran → 5-Bromo-2-phenyl-4-thiazolecarboxylic acid

https://huagongshe.com/reaction/1182675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBromineHCID 24408—
Reactant2-Phenyl-4-carboxythiazoleHCID 138928—
ReactantButyllithiumHCID 178418339—
SolventCyclohexaneHCID 8078—
Product5-Bromo-2-phenyl-4-thiazolecarboxylic acidHCID 66769715—

Reaction Steps

To a solution of 2-phenyl-1,3-thiazole-4-carboxylic acid (3.2 g) in abs. THF (190 mL) was added at 78° C. over 10 min n-BuLi (25 mL, 1.6M in hexanes). After addition, Br2 (1.3 mL) in cyclohexane (7.4 mL) was added over 10 min. The reaction mixture was allowed to warm up to RT and was stirred at this temperature for 3 h. The reaction mixture was then cooled to 0° C., carefully quenched with HCl (1M, 32 mL) and extracted with EtOAc (2×). The combined org. phases were washed with aq. sodium thiosulfate (20%), dried over MgSO4 and evaporated to dryness to give 4.5 g of the desired product. The crude was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664203B2
Source datasetuspto-grants-2014_03
ORD IDord-8d0f46c900804d8785f0fd842c6b5a03
Source noteuspto-grants-2014_03