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HRID 917978Erstellt: 27. Oktober 2026

Hydrogen Bromide → 2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazole

https://huagongshe.com/reaction/917978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktSodium HydroxideHCID 14798—
Edukt1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-HCID 82634—
EduktSodium BisulfiteHCID 23665763—
EduktSodium NitriteHCID 23668193—
KatalysatorCopperHCID 23978—
Produkt2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 12874685—

Reaktionsschritte

To a rapidly stirred suspension of copper bronze (6.1 g.) in 48% HBr (975 ml.) was added over a 1 hour period and cooling to -15° a mixture of NaNO2 (195 g., 2.83 mol.) and 2-amino-5-trifluoromethyl-1,3,4-thiadiazole (103 g., 0.61 mol.) [I. Lalezari and N. Sharghi, J. Hetero. Chem. 3:336 (1966)]. The resultant mixture was stirred for 0.75 hour with ice bath cooling and for 1.5 hour without cooling. The mixture was adjusted to pH 8 using 50% NaOH and maintaining the temperature below 20°. Saturated sodium bisulfite was added until a negative starch-iodide test was obtained. The mixture was made strongly acidic with HCL and extracted with petroleum ether. The extracts were washed with water, dried (MgSO4) and evaporated to the product. Distillation gave 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole; b.p 56°-57°/11 mm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03968226
Quelldatensatzuspto-grants-1976_07
ORD IDord-d3384256036f4e389ecb6c026a676236
Quellennotizuspto-grants-1976_07