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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175782Generated: November 3, 2026

1,5-Bis(2-hydroxyphenyl)-1,4-pentadien-3-one → HCID 136381055, compound

https://huagongshe.com/reaction/1175782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Bis(2-hydroxyphenyl)-1,4-pentadien-3-oneHCID 98176—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventChloroform methanolHCID 21584188—
ProductHCID 136381055HCID 13638105586%

Reaction Steps

Methoxyl-amine hydrochloride (30-35 wt % in H2O, 0.30 mL, 1.12 mmol) was added in one portion to a solution of 1,5-bis(2-hydroxyphenyl)penta-1,4-dien-3-one (EF1) in methanol/CHCl3 (2/3) (5 mL). The reaction proceeded at room temperature for 24 hrs, then additional methoxylamine hydrochloride (0.15 mL, 0.56 mmol) was added and the reaction stirred for an additional 24 hrs. After completion (TLC) the solvent was evaporated, the residue dissolved in methanol, stirred with silica gel and purified after concentration by chromatography on silica gel using 30% EtOAc/hexanes. The product was obtained as a pale yellow foam (86%). 1H NMR (400 MHz, CDCl3) δ 7.56 (1H, dd, J=8.0 Hz, J=1.6 Hz), 7.48 (1H, dd, J=8.0 Hz, J=1.6 Hz), 7.41 (1H, d, J=16.0 Hz), 7.39 (1H, d, J=16.8 Hz), 7.28 (1H, d, J=16.8 Hz), 7.20-7.13 (2H, m), 6.97-6.90 (2H, m), 6.94 (1H, d, J=16.0 Hz), 6.80 (1H, dd, J=8.0 Hz, J=1.6 Hz), 5.53 (1H, s-br), 5.36 (1H, s-br), 4.02 (3H, s). 13C NMR (100 MHz, CDCl3) δ 155.43, 153.86, 153.70, 132.28, 130.25, 130.10, 129.71, 128.00, 127.91, 124.16, 123.88, 123.57, 121.40, 121.30, 118.45, 116.37, 116.33, 62.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842705B2
Source datasetuspto-grants-2010_11
ORD IDord-6feadd004ed84c5eae15f9afdb2aef56
Source noteuspto-grants-2010_11