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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044753Generated: October 26, 2026

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

https://huagongshe.com/reaction/1044753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-oneHCID 57562813—
SolventEthylene GlycolHCID 174—
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 (16.22 g, 78.71 mmol) in ethylene glycol (85 mL) was treated with trimethylorthoformate (18 mL, 164.19 mmol) followed by LiBF4 (1.51 g, 15.74 mmol). The reaction mixture was heated at 95° C. for 2 days. Sat. aq. NaHCO3 was added and the mixture was extracted with Et2O (3×). The org. extracts were washed with brine, 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 solid. TLC:rf (1:1 hept-EA)=0.63. LC-MS-conditions 02: tR=0.89 min; [M+H]+=250.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-310be4375919419b9130be1b8e51e298
Source noteuspto-grants-2013_10