Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42837Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/42837

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktNitrogenHCID 947—
EduktTrimethyl orthoformateHCID 9005—
Edukt1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-oneHCID 57562813—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66820078—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536209B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-47e77418a6244000a6972217938b3779
Quellennotizuspto-grants-2013_09