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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1879893Erstellt: 25. Oktober 2026

Formaldehyde → 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile

https://huagongshe.com/reaction/1879893

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Edukt4-Hydroxybenzyl cyanideHCID 26548—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelTolueneHCID 1140—
Produkt2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrileHCID 591662219.757,2%

Reaktionsschritte

To a solution of (4-hydroxyphenyl)acetonitrile (17.3 g, 0.13 mol) in toluene (350 mL) were added paraformaldehyde (39.0 g, 0.43 mmol) and toluene-4-sulfonic acid monohydrate (2.5 g, 13 mmol) at room temperature. The reaction mixture was heated at reflux for 1 hour. 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 Na2SO4 and evaporated under vacuum. The residue was separated by preparative HPLC to give 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile (7.35 g, 32%). 1H NMR (400 MHz, CDCl3) δ 7.07-7.11 (m, 1H), 6.95-6.95 (m, 1H), 6.88 (d, J=11.6 Hz, 1H), 5.24 (s, 2H), 4.89 (s, 2H), 3.67 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08318733B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-5f66244673db4ae092be02795af0f0df
Quellennotizuspto-grants-2012_11