Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 54090920 | HCID 54090920 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladiumcarbon | HCID 14818447 | — |
| Product | HCID 178495701 | HCID 178495701 | — |
Reaction Steps
1.1 g of (R)-[4-[4-(5-methoxymethyl-2-oxo-oxazolidin-3-yl]-phenyl]-cyclohexylidene]-acetonitrile were dissolved in 50 ml of methanol, treated with 0.2 g of 10% Pd-charcoal and hydrogenated at room temperature at normal pressure until the theoretical hydrogen uptake had taken place. The catalyst was filtered off under suction and the filtrate was evaporated in a vacuum. The oily residue was chromatographed over 15 g of silica gel. Elution was carried out with dichloromethane/ethyl acetate 9:1. The fractions which were pure according to thin-layer chromatography were pooled and crystallized from ethyl acetate/hexane. 0.64 g of (R)-[trans-[4-[4-(5-methoxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-cyclohexyl]-acetonitrile was obtained as white crystals of m.p. 90°-91°. ##EQU1##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574055 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-273f2e55dd4c4f2bbc7728900a9678d6 |
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| Source note | uspto-grants-1996_11 |
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