HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43218Generated: October 26, 2026
4,7-Dibromo-2,1,3-benzothiadiazole → 3,6-Dibromobenzene-1,2-diamine
https://huagongshe.com/reaction/43218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,7-Dibromo-2,1,3-benzothiadiazole | HCID 626361 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,6-Dibromobenzene-1,2-diamine | HCID 11821532 | 66.4% |
Reaction Steps
NaBH4 (26 g, 680 mmol, 10 equiv) was added portionwise (2 h) to a vigorously stirred suspension of 4,7-dibromo-benzo[1,2,5]thiadiazole (Step 179.7) (20 g, 68.0 mmol) in EtOH (400 mL), under a nitrogen atmosphere and keeping the internal temperature below 15° C. The reaction mixture was allowed to warm to 30° C., stirred for 1 h, cooled to 5° C., quenched by addition of H2O (50 mL), and concentrated. The residue was diluted with Et2O/H2O. The resulting suspension was filtered and the filtrate extracted with Et2O. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was triturated in hexane to provide 12 g of the title compound as a white solid: ESI-MS: 263/265/267 [M−H]−; tR=4.20 min (System 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536175B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-d1709645b07944c4b9477092e0b7297b |
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| Source note | uspto-grants-2013_09 |
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