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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42837Generated: October 25, 2026

Ethylene Glycol → 2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazole

https://huagongshe.com/reaction/42837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
Reactant1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-oneHCID 57562813—
SolventSodium BicarbonateHCID 516892—
Product2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66820078—

Reaction Conditions

Temperature95 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and a condenser under inert atmosphere (N2), a solution of 1-(2-bromo-thiazol-5-yl)-ethanone (2.20 g, 10.68 mmol) in ethylene glycol (11.46 mL, 205.53 mmol) was treated with trimethylorthoformate (2.39 mL, 21.76 mmol) followed by LiBF4 (204 mg, 2.14 mmol). The reaction mixture was heated at 95° C. for 2 days. Sat. aq. NaHCO3 (50 mL) was added and the mixture was extracted with EA (50 mL). The org. extracts were washed with brine (2×50 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 to 3:1 hept-EA) gave the title compound as a yellow oil. TLC:rf (1:1 hept-EA)=0.80. LC-MS-conditions 01: tR=0.84 min; [M+H]+=251.85.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-47e77418a6244000a6972217938b3779
Source noteuspto-grants-2013_09