Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-boranyl-N-methylmethanamine | HCID 74604 | — |
| Edukt | 6-Amino-6-desoxy-L-sorbose hydrochloride | HCID 86739032 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Deoxynojirimycin | HCID 29435 | — |
Reaktionsschritte
50 g (0.23 mol) of 6-amino-6-desoxy-L-sorbose hydrochloride were dissolved in 500 ml of distilled water, and the solution was added in the course of one hour to a solution of 11.2 g of dimethylaminoborane in 500 ml of distilled water, whilst stirring at a temperature of 50° C. The mixture was stirred for one hour at room temperature and one hour at 50° C., 5 ml of triethylamine were added to it, and it was then poured over a column containing 800 ml of strongly basic ion exchanger ("Lewatit" MP 500 OH- -form). The exchanger was washed with distilled water, and the runnings collected were concentrated to a syrup on a rotary evaporator. The concentrated syrup was crystallised at 50° C., with addition of a large amount of ethanol. The suspension of crystals was cooled and filtered off under suction, and the crystalline product was dried in a vacuum drying cabinet.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04611058 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-e937e1966cc341faa74ddbac9b485492 |
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| Quellennotiz | uspto-grants-1986_09 |
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