Hydrochloric Acid → 3-(Chloromethyl)benzo(b)thiophene
Reaktionsgleichung
[ClH:1].[CH:2]1[CH:3]=[CH:4][C:5]2[S:10][CH:9]=[CH:8][C:6]=2[CH:7]=1.[CH2:11]=O>O>[Cl:1][CH2:11][C:8]1[C:6]2[CH:7]=[CH:2][CH:3]=[CH:4][C:5]=2[S:10][CH:9]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
HCl (g) was bubbled vigorously through a mixture of thianaphthene (17.0 g, 126.68 mmol), 37% aq. formaldehyde (15 mL) and conc HCl (15 mL) until the reaction temperature rose to 65° C. At this time, the flow of HCl gas was reduced to a slow stream which was maintained for 1.5 hour. The reaction mixture was diluted with H2O (50 mL) and subsequently extracted with ether (2×50 mL). The combined ethereal extracts were dried over Na2SO4 and concentrated under reduced pressure to yield 1 as a straw colored liquid 21.0 g (90.7%). 1H NMR (CDCl3) δ4.90 (s, 2, CH2 --C1), 7.25 (s, 1, CH--S), 7.45 (m, 2, phenyl), 7.88 (m, 2, phenyl).