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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255575Generated: November 1, 2026

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

https://huagongshe.com/reaction/1255575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-(3-Hydroxyphenyl)acetonitrileHCID 13781042—
SolventTolueneHCID 1140—
Product2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrileHCID 5916621647.9%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461156B2
Source datasetuspto-grants-2013_06
ORD IDord-4189ee4115ac408ead546cf8fea8f275
Source noteuspto-grants-2013_06