HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496161Erstellt: 23. Oktober 2026
Ethylacrolein → 2-((2-Benzoylphenylthio)methyl)butyraldehyde
https://huagongshe.com/de/reaction/496161
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylacrolein | HCID 70203 | — |
| Edukt | 2-Mercaptobenzophenone | HCID 3499713 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-((2-Benzoylphenylthio)methyl)butyraldehyde | HCID 22325223 | 64% |
Reaktionsschritte
To an ice bath cooled solution of 9.76 g (0.116 mole) of 2-ethylacrolein in 40 mL of dry THF was added 24.6 g (0.116 mole) of 2-mercaptobenzophenone in 40 mL of THF followed by 13 g (0.128 mole) of triethylanine. The reaction mixture was stirred at room temperature for 3 days, diluted with ether, and was washed successively with dilute HCl, brine, and 1 M potassium carbonate. The ether layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by HPLC (10% EtOAc-hexane) to give 22 g (64%) of 11 in the second fraction. An attempt to further purifiy this material by kugelronr distillation at 0.5 torr (160-190° C.) gave a fraction (12.2 g) which contained starting material indicating a reversed reaction during distillation. This material was dissolved in ether (100 mL) and was washed with 50 mL of 1 M potassium carbonate three times to give 6.0 g of a syrup which was purified by HPLC (10% EtOAc-hexane) to give 5.6 g of pure 11.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06943189B2 |
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| Quelldatensatz | uspto-grants-2005_09 |
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| ORD ID | ord-82ef325b99484b92b22692152b474b38 |
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| Quellennotiz | uspto-grants-2005_09 |
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