HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854661Generated: October 27, 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/1854661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | Boron trioxide | HCID 518682 | — |
| Reactant | 4-Diethylamino-2-(methoxymethoxy)benzaldehyde | HCID 14387675 | — |
| Reactant | 6-(4-Hydroxy-3-methoxyphenyl)hex-5-ene-2,4-dione | HCID 54318819 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | (1E,6E)-1-[4-diethylamino-2-(methoxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione | HCID 68552476 | 159.5% |
Reaction Steps
6-(4-Hydroxy-3-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 extract 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 (61.5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962674B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-3f77e5207c724258b2d19af14a890e77 |
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| Source note | uspto-grants-2015_02 |
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