Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175781Generated: November 2, 2026

1,5-Bis(2-hydroxyphenyl)-1,4-pentadien-3-one → HCID 68698394, compound

https://huagongshe.com/reaction/1175781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Bis(2-hydroxyphenyl)-1,4-pentadien-3-oneHCID 98176—
ReactantSodium borohydrideHCID 4311764—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 68698394HCID 6869839466%

Reaction Steps

To a solution of 1,5-bis(2-hydroxyphenyl)penta-1,4-dien-3-one (EF1) (109 mg, 0.41 mmol) in THF/methanol (10/1) (2.5 mL) was added NaBH4 (40 mg, 1.30 mmol) in one portion at 0° C. After stirring for 30 min at this temperature the reaction was quenched with H2O dist and cold brine, diluted with Et2O (10 mL) and neutralized by bubbling CO2 through the dark-red solution (color change to pale yellow). The aqueous phase was extracted with ether, the combined ether layers washed with brine, dried over MgSO4 and concentrated. The crude product was purified by chromatography on silica gel using 30% EtOAc/hexanes. The product was obtained as a white solid (66%). 1H NMR (300 MHz, CDCl3) δ 7.27 (2H, dd, J=8.0 Hz, J=2.4 Hz), 7.21 (1H, s-br), 7.14-7.06 (3H, m), 6.90-6.83 (3H, m), 6.80-6.74 (2H, m), 6.18 (1H, dd, J=20.8 Hz, J=8.8 Hz), 5.99 (1H, s-br), 4.24 (1H, t-deformed), 3.23 (1H, s-br), 2.86 (1H, m), 2.71 (1H, m), 1.91 (2H, m). 13C NMR (75 MHz, CDCl3) δ 154.25, 152.96, 132.84, 130.75, 129.03, 127.79, 127.62, 127.46, 125.71, 123.97, 121.12, 121.07, 116.42, 116.22, 72.09, 37.57, 25.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842705B2
Source datasetuspto-grants-2010_11
ORD IDord-7c9d03e342de4c0bb20e3aea4c80d04b
Source noteuspto-grants-2010_11