HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253187Generated: October 29, 2026
Hydrogen Bromide → 2-Bromo-5-phenyl-1,3,4-thiadiazole
https://huagongshe.com/reaction/253187
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2-amino-5-phenyl-1,3,4-thiadiazole sulfate salt | HCID 16213087 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-5-phenyl-1,3,4-thiadiazole | HCID 13104117 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872010B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-1742f78049334d6885a6f18a49f66fd4 |
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| Source note | uspto-grants-2011_01 |
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