Hydrogen Bromide → 4-(2-Bromoethyl)phenol
Reaktionsgleichung
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][CH2:7]O)=[CH:4][CH:3]=1.[BrH:11]>O>[Br:11][CH2:7][CH2:6][C:5]1[CH:9]=[CH:10][C:2]([OH:1])=[CH:3][CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
(4-Hydroxyphenethyl) alcohol (1.50 g, 0.01086 mol) and 48 wt. % hydrobromic acid (10 ml) were heated at 100° C. for 1.5 h. After being cooled, the reaction mixture was poured into water and extracted with ethyl acetate. The extracts were washed with water, dried and concentrated in vacuo to give a raw product. Purification by flash chromatography (heptane/ethyl acetate 9:1) gave a pure product (2.01 g, 92%). 1H NMR (400 MHz, DMSO-d6): 2.99 (2H, t, 3J=7.4 Hz), 3.63 (2H, t, 3J=7.4 Hz), 6.68 (2H, d, 3J=8.5 Hz), 7.05 (2H, d, 3J=8.3 Hz), 9.24 (1H, s, —OH).
Aufarbeitung
- temperatureAfter being cooled
- extractionextracted with ethyl acetate
- washThe extracts were washed with water
- customdried
- concentrationconcentrated in vacuo
- customto give a raw product
- customPurification by flash chromatography (heptane/ethyl acetate 9:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-9609a09fd22149698b73eed8b1367578
- Quelldatensatz
- uspto-grants-2008_06
- Patentnummer
- US07390923B2
Notizen zur Reaktion
Wird geladen…