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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836002Generated: October 31, 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/1836002

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 numberUS06774248B2
Source datasetuspto-grants-2004_08
ORD IDord-119e9de673fc46f2a2d4082a151b49b6
Source noteuspto-grants-2004_08