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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917978Generated: October 25, 2026

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

https://huagongshe.com/reaction/917978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-HCID 82634—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
Product2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazoleHCID 12874685—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03968226
Source datasetuspto-grants-1976_07
ORD IDord-d3384256036f4e389ecb6c026a676236
Source noteuspto-grants-1976_07