Water → 2-Bromo-1,3-benzothiazol-6-ol
Reaktionsgleichung
[Br:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11]C)[CH:8]=[CH:7][C:5]=2[N:6]=1.B(Br)(Br)Br.O>ClCCl>[Br:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:5]=2[N:6]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 2-bromo-6-methoxybenzothiazole (0.67 g) in dry dichloromethane (30 ml) at ambient temperature under an atmosphere of nitrogen was added dropwise a solution of boron tribromide in dichloromethane (5.5 ml, 1M). The mixture was stirred for 2 hours at ambient temperature, stored for 2 days then poured into water. The organic phase was separated, washed with water, dried over magnesium sulphate then evaporated under reduced pressure to give 2-bromo-6-hydroxybenzothiazole as a pale pink solid, 0.60 g, m.p. 203-204° C.
Aufarbeitung
- waitstored for 2 days
- customThe organic phase was separated
- washwashed with water
- dry with materialdried over magnesium sulphate
- customthen evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-2a2ec4c282ac4da392f2ccb81d1b9f37
- Quelldatensatz
- uspto-grants-2011_11
- Patentnummer
- US08067592B2
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