Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Glycinate | HCID 26066 | — |
| Edukt | Methan(2H)ol | HCID 123113 | — |
| Edukt | (-)-10,2-Camphorsultam | HCID 658384 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Glycylbornane-10,2-sultam | HCID 70275055 | 158,7% |
Reaktionsschritte
Over 20 minutes, 2 M trimethylaluminum in hexane (40 ml, 1.2 eq) was added to (2R)-bornane-10,2-sultam (15.7 g, 1.1 eq) in toluene (110 ml) at 0° C., then left for 30 minutes. Ethyl N-(diphenylmethylene)[1,2-13C2, 15N, 2,2-2H2]glycinate (18.1 g, 66.4 mmol) in toluene (10 ml) was added and the reaction stirred overnight. Heating to 50° C. for 3-4 hours drove the reaction to completion. Workup was effected by cooling the reaction in ice and carefully adding MeOD (20 ml). After 1 hour, D2O (30 ml) was carefully added. Filtering, extracting with ethyl acetate (2×250 ml), drying over MgSO4 and purifying by silica gel flash chromatography (Hexane: Ethyl Acetate 10:1 to 1:1) gave (2R)-N-(diphenylmethylene)[1,2-13C2, 15N, 2,2-2H2]glycylbornane-10,2-sultam (28.7 g, 99% yield) as an orange oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06376253B1 |
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| Quelldatensatz | uspto-grants-2002_04 |
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| ORD ID | ord-efcf14a594d8494386a51a0b4f712840 |
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| Quellennotiz | uspto-grants-2002_04 |
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