Benzoyl Peroxide → HCID 21866262, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:6]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][C:8]=2[CH3:14])=[N:5][S:4][N:3]=1.C1C(=O)N([Br:22])C(=O)C1.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:22][CH2:14][C:8]1[CH:9]=[C:10]([Cl:13])[CH:11]=[CH:12][C:7]=1[C:6]1[C:2]([Cl:1])=[N:3][S:4][N:5]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
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).
Aufarbeitung
- temperaturewere refluxed for 1 h
- temperaturethe solution was refluxed for a further 16 h
- filtrationThe resulting suspension was filtered
- washrinsing with ether
- washThe filtrate was washed with 10% aqueous sodium sulfite, saturated aqueous sodium bicarbonate solution and brine
- customThe ether layer was separated
- dry with materialdried (Na2SO4)
- customThe residue was purified by flash chromatography on silica (eluting with EtOAc/hexanes gradient, 1–3% EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-51e9ef4e601840eabeeb99cdb14b040e
- Quelldatensatz
- uspto-grants-2006_12
- Patentnummer
- US07144899B2
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