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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 982465Erstellt: 24. Oktober 2026

Hydrochloric Acid → 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione

https://huagongshe.com/de/reaction/982465

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-oneHCID 383405—
Edukt3-Methylthio4-n-propoxy-5-benzyloxybenzaldehydeHCID 10471022—
Katalysator3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
Produkt1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dioneHCID 10098743—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

175 g 3-methylthio-4-n-propoxy-5-benzyloxybenzaldehyde, 135 g of 3,4,5-trimethoxyphenylvinylketone, 10 g of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide, 25 mL of triethyl amine dissolved in 150 ml of dimethylformamide was heated at 60° C. overnight, and the reaction mixture was treated with 400 mL of 1.5N HCl and the aqueous layer decanted. The residue was treated again with fresh 400 mL of 1.5N HCl and decanted two more times. The remaining residue was crystallized from 400 mL of methanol and washed thoroughly with methanol, hexane, and methanol and dried to yield the title compound as a tan solid: NMR(200 MHz, CDCl3) δ 1.03(t, CH2CH2CH3), 1.82(m, CH2CH2CH3), 2.50(s, SCH3), 3.43(s, C(O)CH2CH2CO), 3.94(s, 3 OCH3), 4.11(t, OCH2CH2CH3), 5.17(s, OCH2Ar), 7.30-7.52(m, ArH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04996203
Quelldatensatzuspto-grants-1991_02
ORD IDord-6281e817a89f44aa85263744adfdab80
Quellennotizuspto-grants-1991_02