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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-one | HCID 383405 | — |
| Edukt | 3-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde | HCID 10471022 | — |
| Katalysator | 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide | HCID 9964923 | — |
| Produkt | 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione | HCID 10098743 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04996203 |
|---|
| Quelldatensatz | uspto-grants-1991_02 |
|---|
| ORD ID | ord-6281e817a89f44aa85263744adfdab80 |
|---|
| Quellennotiz | uspto-grants-1991_02 |
|---|