Hydrogen Bromide → alpha-(2-Bromoethyl)-3,4-dichlorophenylacetic acid
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]2[CH2:13][CH2:12][O:11][C:10]2=[O:14])[CH:5]=[CH:6][C:7]=1[Cl:8].[BrH:15]>CC(O)=O>[Br:15][CH2:12][CH2:13][CH:9]([C:4]1[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=1)[C:10]([OH:11])=[O:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Treat the product of Step 1 (21.25 g, 91.96 mmoles) at room temperature with 130 ml. of HOAc saturated with HBr gas. Stir at room temperature for 2 days, then pour into 800 ml. of ice-water with stirring. Store the resultant gum in a freezer for two days, then decant the liquid from the solidified gum. Triturate the solid, filter, wash with water and air dry. Yield: 26.2 g (m.p.=80°-81° C.).
Aufarbeitung
- additionpour into 800 ml
- waitStore the resultant gum in a freezer for two days
- customdecant the liquid from the solidified gum
- customTriturate the solid
- filtrationfilter
- washwash with water and air
- customdry
Quellen und Nachweise
- ORD-Eintrag
- ord-68cbea09f04e4df697ebef1c7de3a156
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840725
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