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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1044753Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1044753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktTrimethyl orthoformateHCID 9005—
EduktSodium BicarbonateHCID 516892—
Edukt1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-oneHCID 57562813—
LösungsmittelEthylene GlycolHCID 174—
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 (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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08563714B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-310be4375919419b9130be1b8e51e298
Quellennotizuspto-grants-2013_10