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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231915Generated: October 26, 2026

Acrylonitrile → 7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrile

https://huagongshe.com/reaction/2231915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantDabcoHCID 9237—
Reactant4-Benzyloxy-2-hydroxybenzaldehydeHCID 561235—
Product7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrileHCID 1432975845.7%

Reaction Steps

A mixture of 1.14 g of 4-benzyloxy-2-hydroxybenzaldehyde, 0.125 g of 1,4-diazabicyclo[2,2,2]octane and 0.65 g of acrylonitrile was stirred and heated at 80°-85° C., under argon, for 2 hours. After removal of the solvent, the residual product was dissolved in tetrahydrofuran-ether(1:1), washed with 1N-sodium hydroxide, water, dried, and the solvents evaporated in vacuo. The crude material (1.10 g) was purified by column chromatography on silica gel to afford 0.6 g (45.7%) of 7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrile, as a colorless solid mp 95°-98° C. (from ethyl acetatehexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04785017
Source datasetuspto-grants-1988_11
ORD IDord-bcdc5da70e454db4af5f3632e112fd17
Source noteuspto-grants-1988_11