HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16645Erstellt: 25. Oktober 2026
Water → Ethyl 6-(2-isobutoxy-5-methoxyphenyl)-6-oxo-3-methylhexa-2,4-dienoate
https://huagongshe.com/reaction/16645
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ethyl (2E)-3-methyl-4-oxo-2-butenoate | HCID 6009828 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | HCID 86603586 | HCID 86603586 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 6-(2-isobutoxy-5-methoxyphenyl)-6-oxo-3-methylhexa-2,4-dienoate | HCID 86603585 | — |
Reaktionsschritte
3 g (8.4 mmol) of ethyl [2-(2-isobutoxy-5-methoxyphenyl)-2-oxoethyl]-phosphonate dissolved in 20 ml of tetrahydrofuran are added dropwise to a suspension of 1.41 g (12.6 mmol) of potassium tert-butoxide in 30 ml of tetrahydrofuran, heated to 50° C. Heating is continued for 20 minutes at 50° C., the mixture is then cooled to 0° C. and 1.8 g (12.6 mmol) of ethyl 3-methyl-4-oxocrotonate dissolved in 20 ml of tetrahydrofuran are added dropwise. The reaction mixture is then stirred for 72 hours at 25° C. Water is added and the resulting mixture is extracted with ether. After drying (Na2SO4), the solvent is evaporated off and the residue is purified by flash chromatography (dichloromethane) (2.58 g of yellow oil; 89%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737176B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-a324b16e61e64ab7b1a0c8ce6fe558cf |
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| Quellennotiz | uspto-grants-2010_06 |
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