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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794500Generated: November 3, 2026

3-[5-Hydroxy-2-(4-hydroxyphenyl)-benzofuran-7-yl]-acrylamide → 3-[5-Hydroxy-2-(4-hydroxy-phenyl)-benzofuran-7-yl]-acrylonitrile

https://huagongshe.com/reaction/1794500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[5-Hydroxy-2-(4-hydroxyphenyl)-benzofuran-7-yl]-acrylamideHCID 68845196—
SolventDimethylformamideHCID 6228—
SolventPhosphorus oxychlorideHCID 24813—
Product3-[5-Hydroxy-2-(4-hydroxy-phenyl)-benzofuran-7-yl]-acrylonitrileHCID 6884069310.5%

Reaction Steps

A solution of 3-[5-hydroxy-2-(4-hydroxyphenyl)-benzofuran-7-yl]-acrylamide 61 (0.07 g, 0.24 mmol) in DMF (5 mL) and phosphorous oxychloride (0.11 mL) was heated at 65° C. for 2 hours. Then ice was added to the reaction mixture and the product extracted into ethyl acetate. The organic layer was dried over MgSO4 and the solvent removed in vacuo. The crude product was submitted for reverse phase prep HPLC. The product was isolated to give 0.007 g of 3-[5-hydroxy-2-(4-hydroxy-phenyl)-benzofuran-7-yl]-acrylonitrile 64: 1H NMR (DMSO-d6) δ 9.90 (s, 1 H), 9.48 (s, 1 H), 7.82 (d, 2 H, J=8.6 Hz), 7.79 (d, 1 H, J=16.7 Hz), 7.13 (s, 1 H), 7.03 (d, 1 H, J=2.3 Hz), 6.92 (d, 1 H, J=2.4 Hz), 6.88 (d, 2 H, J=8.7 Hz), 6.71 (d, 1 H, J=16.8 Hz); MS 276 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022733B2
Source datasetuspto-grants-2006_04
ORD IDord-98b2bf75882f4df1bba4954ec7561d0c
Source noteuspto-grants-2006_04