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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747926Generated: November 1, 2026

Hydrogen Bromide → 2-Bromo-5-phenyl-1,3,4-thiadiazole

https://huagongshe.com/reaction/747926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2-amino-5-phenyl-1,3,4-thiadiazole sulfate saltHCID 16213087—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Bromo-5-phenyl-1,3,4-thiadiazoleHCID 1310411774%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 2-amino-5-phenyl-1,3,4-thiadiazole sulfate (Aldrich, 2.5 g, 9.08 mmol) and 48% aqueous HBr (10 mL) was cooled to 5° C. and a solution of NaNO2 (0.69 g, 9.99 mmol) H2O (10 mL) was added dropwise at a rate so the internal temperature is maintained at approximately 5° C. The mixture was stirred for 15 min after the addition, then CuBr (0.69 g, 4.8 mmol) was added portion-wise so as to maintain the temperature at approximately 5° C. After the addition was complete, the mixture was allowed to warm to ambient temperature and stirred for 16 h. The mixture was diluted with 20 mL CH2Cl2 and 10 mL H2O. The organic layer was separated and concentrated under reduced pressure to provide the title compound (1.63 g, 6.76 mmol, 74% yield). MS (DCl/NH3) m/z 241, 243 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399765B2
Source datasetuspto-grants-2008_07
ORD IDord-3b15d66f1a9540cdb4d2a07549298b33
Source noteuspto-grants-2008_07