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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854662Generated: November 3, 2026

Butylamine → (1E,6E)-1-[4-diethylamino-2-(methoxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione

https://huagongshe.com/reaction/1854662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantTributyl borateHCID 12712—
ReactantBoron trioxideHCID 518682—
Reactant4-Diethylamino-2-(methoxymethoxy)benzaldehydeHCID 14387675—
Reactant6-(3-Hydroxy-4-methoxyphenyl)hex-5-ene-2,4-dioneHCID 57084921—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product(1E,6E)-1-[4-diethylamino-2-(methoxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dioneHCID 68552476149.9%

Reaction Steps

6-(3-Hydroxy-4-methoxyphenyl)hex-5-ene-2,4-dione (20 mg, 0.085 mmol) and boron trioxide (11 mg, 0.16 mmol) were placed in a 20 mL reaction vessel, and dissolved in 0.4 mL of ethyl acetate. To the stirring solution at 80° C. was added a solution of 4-diethylamino-2-(methoxymethoxy)benzaldehyde (26 mg, 0.11 mmol) and tri-n-butyl borate (25 μL, 93 μmol) in 0.7 mL of ethyl acetate. After the reaction mixture was stirred for 2 h at the same temperature, n-butylamine (10 μL, 0.10 mmol) was added with additional stirring for 1 h. The resulting mixture was diluted with 25 mL of brine, and the solution was extracted with 50 mL of ethyl acetate. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to give a crude solid of (1E,6E)-1-[4-diethylamino-2-(methoxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione (57.8 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962674B2
Source datasetuspto-grants-2015_02
ORD IDord-1262e27b587f4618a669b06dda5fb1f2
Source noteuspto-grants-2015_02