Reaktionsgleichung
[F:1][C:2]([F:11])([F:10])[C:3]1[S:4][CH:5]=[C:6]([CH2:8]O)[N:7]=1.P(Br)(Br)[Br:13]>C(Cl)Cl>[Br:13][CH2:8][C:6]1[N:7]=[C:3]([C:2]([F:11])([F:10])[F:1])[S:4][CH:5]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirring solution of (2-(trifluoromethyl)thiazol-4-yl)methanol (550 mg, 3.00 mmol) in DCM (5 ml) was added PBr3 (0.283 ml, 3.00 mmol) at 0-5° C. in 5-10 min. and stirring continued for 1 h. Reaction mixture was diluted with DCM and washed with water. Organic layer was separated and distilled out to get crude product which was column purified using 0-2% EtOAC in hexane to get title compound in 36% yield.
Aufarbeitung
- customReaction mixture
- washwashed with water
- customOrganic layer was separated
- distillationdistilled out
- customto get crude product which
- custompurified
Quellen und Nachweise
- ORD-Eintrag
- ord-b2c90fe60bc649b0aa3bc4837e7703bb
- Quelldatensatz
- uspto-grants-2016_07
- Patentnummer
- US09394300B2
Verknüpfte Notizen
Wird geladen…