HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839947Generated: October 25, 2026
Hydrogen Bromide → 2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazole
https://huagongshe.com/reaction/839947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)- | HCID 82634 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazole | HCID 12874685 | 87% |
Reaction Steps
A solution of 69 g (1.0 mole) of sodium nitrite in 150 ml of water was added dropwise over the course of 1.5 hours, while stirring, to a solution, cooled to +5° C, of 84.5 g (0.5 mole) of 2-amino-5-trifluoromethyl-1,3,4-thiadiazole in a mixture of 400 ml of hydrogen bromide (48% strength) and 100 ml of water. Thereafter, the evolution of the nitrous gases and of the nitrogen was completed by stirring at 25° C (1 hour). The product separated out as a dark brown, heavy liquid and was abstracted from the reaction mixture by repeated extraction with a total of 500 ml of methylene chloride. After washing with 2 × 100 ml of water, drying over sodium sulfate and careful distillation of the solvent, the residue was fractionated in vacuo through a short column. 101 g (87% of theory) of 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole of boiling point 55° C/10 mm Hg were obtained. ##STR80##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04097669 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-590395cb16104f2e9105cd5fe4d4a8a9 |
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| Source note | uspto-grants-1978_06 |
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