HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1040328Erstellt: 25. Oktober 2026
Methanol → (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde
https://huagongshe.com/reaction/1040328
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Edukt | (2E)-3-(2,6-dimethoxyphenyl)acrylonitrile | HCID 59658521 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde | HCID 23928193 | 60% |
Reaktionsschritte
Add 355 mL of a 1M solution of diisobutylaluminium hydride (DIBAL-H) (355 mmol) in toluene to a solution of 61 g (322 mmol) of (2E)-3-(2,6-dimethoxyphenyl)acrylonitrile in 600 mL of anhydrous toluene under argon and cooled to 0° C., maintaining the temperature at 0° C. Then bring the reaction mixture to room temperature (RT) and stir for 3 h. Then add 13 mL (322 mmol) of methanol and then, dropwise, 170 g (174 mmol) of an aqueous solution of sulphuric acid at 10 wt. %. Stir the suspension for one hour, then filter on a celite bed. Wash the filtrate with 500 mL of water then dry over Na2SO4 and concentrate under reduced pressure. Take up the residue obtained in 500 mL of DCM and filter in a silica column, eluting with DCM. After concentration under reduced pressure, we obtain 37 g of (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde in the form of colourless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08552201B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-088b344ef0ad49559dc9a20036affd12 |
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| Quellennotiz | uspto-grants-2013_10 |
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