HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3989Erstellt: 24. Oktober 2026
2,3-Dihydroxybutanedioic Acid → 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde
https://huagongshe.com/de/reaction/3989
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 5-[Methyl(2-phenylethyl)amino]-2-phenyl-2-propan-2-ylpentanenitrile | HCID 71225 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde | HCID 88638019 | — |
Reaktionsschritte
180 ml of a 1M solution of diisobutylaluminum hydride in hexane were added dropwise, at -5° C., to a solution of 33.4 g (0.1 mole) of 2-[3-[(phenylethyl)-methylamino]-propyl]-isopropylphenylacetonitrile in 400 ml of diethyl ether. The mixture was stirred for 1.5 hours, after which 500 ml of 10% strength sulfuric acid were added. 30 g of tartaric acid were introduced, the mixture was rendered alkaline with concentrated potassium hydroxide solution, and the ether phase was separated off and washed several times with sodium chloride solution. After the ether phase had been dried over sodium sulfate, the ether was distilled off, the remaining oily residue was dissolved in 300 ml of ethyl acetate, and hydrochloric acid in isopropanol was added. The mixture was left to stand overnight, after which the precipitated hydrochloride was filtered off under suction.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04723039 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-9e27edb996dc4b2e8698c669aeab451a |
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| Quellennotiz | uspto-grants-1988_02 |
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