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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230031Erstellt: 23. Oktober 2026

Sodium Hydroxide → 5-Bromo-2-formylaminomethylthiazole

https://huagongshe.com/de/reaction/230031

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktBromineHCID 24408—
EduktSodium SulfiteHCID 24437—
EduktSodium BromideHCID 253881—
EduktFormamide, N-(2-thiazolylmethyl)-HCID 22916723—
EduktSodium Phosphate, Monobasic, DihydrateHCID 23673460—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-2-formylaminomethylthiazoleHCID 2308876233,6%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

2-Formylaminomethylthiazole (200 g) was added to a solution of 4.5 kg of sodium dihydrogenphosphate dihydrate in 6 L of water, and the mixture was stirred at 30° C. Sodium bromide (4.0 kg) and 2 L of tetrahydrofuran were added thereto in that order. Bromine (1.49 kg) was added while adjusting the solution to pH 3 by the addition of a 6 N aqueous sodium hydroxide solution, and the mixture was stirred for 2 hr. The reaction mixture was added to a solution of 500 g of sodium sulfite in 4 L of water to stop the reaction and was then adjusted to pH 4.9 by the addition of a 6 N aqueous sodium hydroxide solution while maintaining the temperature of the mixture at 30° C. The reaction mixture was extracted with 10 L of ethyl acetate and then with 5 L of ethyl acetate. The organic layers were combined and were dried over anhydrous magnesium sulfate. The solvent was removed to bring the volume to 1 L, and the concentrate was stirred at 6° C. for 12 hr for crystallization to give 104.4 g of 5-bromo-2-formylaminomethylthiazole. The results of NMR analysis were in agreement with the results of analysis in Example 3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563901B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-38e4c5a8df834501bcd5cf4e974baea1
Quellennotizuspto-grants-2009_07