Reaktion #46222

Reaktionsgleichung

(3-hydroxyphenyl)acetonitrile

paraformaldehyde

toluene-4-sulfonic acid monohydrate

→

2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrile

Ausbeute 47.9%

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe reaction mixture was heated
2. 2
   Temperaturat reflux for 40 minutes
3. 3
   SonstigeToluene was removed by evaporation
4. 4
   workup.ADDITIONWater (150 mL) and ethyl acetate (150 mL) were added
5. 5
   SonstigeThe organic layer was separated
6. 6
   Extraktionthe aqueous layer was extracted with ethyl acetate
7. 7
   WaschenThe combined organics were washed with brine
8. 8
   Trocknendried over anhydrous Na2SO4
9. 9
   Sonstigeevaporated under vacuum
10. 10
    SonstigeThe residue was separated by preparative HPLC

Vorschrift

To a solution of (3-hydroxyphenyl)acetonitrile (75.0 g, 0.56 mol) in toluene (750 mL) was added paraformaldehyde (84.0 g, 2.80 mol) and toluene-4-sulfonic acid monohydrate (10.7 g, 56.0 mmol) at room temperature. The reaction mixture was heated at reflux for 40 minutes. Toluene was removed by evaporation. Water (150 mL) and ethyl acetate (150 mL) were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organics were washed with brine, dried over anhydrous Na2SO4 and evaporated under vacuum. The residue was separated by preparative HPLC to give 2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrile (4.7 g, 5%). 1H NMR (300 MHz, CDCl3) δ 6.85-6.98 (m, 3H), 5.25 (d, J=3.0 Hz, 2H), 4.89 (s, 2H), 3.69 (s, 2H).

Quelle