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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42797Erstellt: 23. Oktober 2026

Ethylene Glycol → 4-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole

https://huagongshe.com/de/reaction/42797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktNitrogenHCID 947—
EduktTrimethyl orthoformateHCID 9005—
Edukt1-(4-Chloromethyl-thiazol-2-yl)ethanoneHCID 66819977—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt4-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66928813—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

In a flame dried round-bottomed flask equipped with a magnetic stir bar and a Dean-Stark apparatus under inert atmosphere (N2), a solution of 1-(4-chloromethyl-thiazol-2-yl)-ethanone (992 mg, 5.65 mmol) in ethylene glycol (6.30 mL, 112.96 mmol) was treated with trimethylorthoformate (1.24 mL, 11.30 mmol) followed by LiBF4 (106 mg, 1.13 mmol). The reaction mixture was heated at 95° C. for 2 h. 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 (4:1 hept-EA) gave the title compound as a yellow oil: TLC:rf (4:1 hept-EA)=0.30. LC-MS-conditions 02: tR=0.84 min, [M+H]+=220.36.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536209B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d2bbcdd6662c4b628c613255c016266f
Quellennotizuspto-grants-2013_09