Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | N-(tert-Butoxycarbonyl)-D-prolinol | HCID 688279 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | HCID 178418287 | HCID 178418287 | — |
| Produkt | N-(tert-Butoxycarbonyl)-D-prolinal | HCID 7009153 | 102% |
Reaktionsschritte
To a water cooled (25° C.) solution of 10.0 g of (R)-2-(hydroxymethyl)-1-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester in 250 ml of dry methylene chloride is added in one portion 16.0 g of pyridinium chlorochromate, 36.0 g of dried, crushed 4Å molecular sieves and 4.5 ml of glacial acetic acid. The resulting mixture is stirred at 25° C. for one hour. Twenty-five grams of diatomaceous earth and 500 ml of diethyl ether is added, the suspension is filtered through a pad of diatomaceous earth and the filtrate concentrated in vacuo. The residue is dissolved in diethyl ether and is passed through a short column of silica gel using diethyl ether as the eluant. The first two 500 ml fractions contain the desired aldehyde. The solvent is concentrated in vacuo to give 10.1 g of desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05001142 |
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| Quelldatensatz | uspto-grants-1991_03 |
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| ORD ID | ord-8639a42bff00433bb8550db28372ba6d |
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| Quellennotiz | uspto-grants-1991_03 |
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