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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238245Generated: October 28, 2026

Sodium borohydride → HCID 68790209, compound

https://huagongshe.com/reaction/2238245

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 numberUS07718682B2
Source datasetuspto-grants-2010_05
ORD IDord-bc72ac8cb84b4660a8c36e23cbf4b4d7
Source noteuspto-grants-2010_05