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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401554Erstellt: 24. Oktober 2026

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

https://huagongshe.com/reaction/401554

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
PatentnummerUS08741933B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-5635d3f93ce34459925a4c2d02184ca9
Quellennotizuspto-grants-2014_06