HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857784Generated: October 29, 2026
Benzoyl Peroxide → HCID 21866262, compound
https://huagongshe.com/reaction/857784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 21866306 | HCID 21866306 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 21866262 | HCID 21866262 | — |
Reaction Steps
A mixture of 3-chloro-4-(4-chloro-2-methylphenyl)-1,2,5-thiadiazole (0.211 g, 0.86 mmol), NBS (0.153 g, 0.86 mmol) and benzoyl peroxide (10.4 mg, 0.04 mmol) in carbon tetrachloride (5.0 mL) were refluxed for 1 h. More benzoyl peroxide (10.4 mg, 0.04 mmol) was added and the solution was refluxed for a further 16 h. The resulting suspension was filtered, rinsing with ether. The filtrate was washed with 10% aqueous sodium sulfite, saturated aqueous sodium bicarbonate solution and brine. The ether layer was separated, dried (Na2SO4) and reduced in vacuo. The residue was purified by flash chromatography on silica (eluting with EtOAc/hexanes gradient, 1–3% EtOAc). 3-[2-(Bromomethyl)-4-chlorophenyl]-4-chloro-1,2,5-thiadiazole was isolated as a yellow oil. 1H NMR (CDCl3, 400 MHz) δ 4.51 (s, 2H), 7.43 (s, 2H), 7.55 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07144899B2 |
|---|
| Source dataset | uspto-grants-2006_12 |
|---|
| ORD ID | ord-51e9ef4e601840eabeeb99cdb14b040e |
|---|
| Source note | uspto-grants-2006_12 |
|---|