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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217608Generated: October 29, 2026

Sodium borohydride → HCID 68790209, compound

https://huagongshe.com/reaction/2217608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3,5-Dimethoxyphenyl)-2-[4-(4-formylphenoxy)-phenyl]-acrylic acid methyl esterHCID 73197847—
SolventEthanolHCID 702—
ProductHCID 68790209HCID 68790209101.9%

Reaction Steps

Compound 9 (5.0 g, 11.9 mmol) was suspended in anhydrous ethanol (60 mL) at room temperature and sodium borohydride (0.23 g, 6.1 mmol) was added with efficient stirring. Reaction was complete in 1 h, solvent was evaporated and the residue was dissolved in ethyl acetate. The organic layer was extracted with water (50 mL), brine (25 mL), dried on anhydrous magnesium sulfate, filtered and solvent was evaporated to yield the title compound 12 as white solid (5.1 g, 100%): mp 93-95° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.72 (s, 1H), 7.35 (d, J=8.8 Hz, 2H), 7.19 (d, J=8.8 Hz, 2H), 7.02 (d, J=8.4 Hz, 2H), 7.00 (d, J=8.4 Hz, 2H), 6.41 (t, J=2.4 Hz, 1H), 6.29 (d, J=2.0 Hz, 2H), 5.18 (t, J=6.4 Hz, 1H), 4.49 (d, J=4.8 Hz, 2H), 3.73 (s, 3H), 3.57 (s, 6H); MS (EI) m/z 315[M]+. Anal. (C25H24O6) C, H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407978B2
Source datasetuspto-grants-2008_08
ORD IDord-07774aacd4c540e4a871d8a3ab2db6ce
Source noteuspto-grants-2008_08