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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157306Generated: October 27, 2026

Ethylene Glycol → 4-Bromo-2-(1,3-dioxolan-2-yl)thiazole

https://huagongshe.com/reaction/1157306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant4-Bromothiazole-2-carboxaldehydeHCID 2763187—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product4-Bromo-2-(1,3-dioxolan-2-yl)thiazoleHCID 5951130394.3%

Reaction Steps

To a rb flask with an attached Dean-Stark trap containing molecular sieves, 4A (0.25g) was added 4-bromothiazole-2-carbaldehyde (4.4 g, 22.91 mmol). The starting material was dissolved in Benzene (45 ml) and Ethylene glycol (1.406 ml, 25.2 mmol) was added followed by pTsOH (0.218 g, 1.146 mmol). The mixture was heated to reflux for 3 h. The mixture was cooled to rt, and was partitioned with sat. aq. NaHCO3. The mixture was washed 2× with sat. NaHCO3 (40 mL), then once with sat. NaCl (40 mL). The organic layer was dried with Na2SO4. The drying agent was removed by filtration, and the mixture was concentrated under reduced pressure. The residue was purified by biotage flash chromatography using a 40+M column and a 0 to 20% EtOAc in hexanes gradient. The product, 4-bromo-2-(1,3-dioxolan-2-yl)thiazole (5.1 g, 21.60 mmol, 94% yield), was collected as a light-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-72e7eafc20644f9c9af87e218ae26cfa
Source noteuspto-grants-2010_10