Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethyl Sulfide | HCID 1068 | — |
| Edukt | Dichloromethane methanol | HCID 21226129 | — |
| Edukt | N-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl ester | HCID 70044917 | — |
| Produkt | HCID 131717895 | HCID 131717895 | — |
Reaktionsschritte
Dissolve N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl ester (13 g, 29.8 mmol ) in methylene chloride/methanol (10:1, 220 mL). Cool to -78° C. and sparge with a mixture of ozone/oxygen for approximately 10 minutes until a blue color persists. Sparge with nitrogen for 10 minutes at -78° C. to remove excess ozone. Treat with methylsulfide (60 mL, 0.82 mol) and allow to warm to room temperature. Stir at room temperature for 2.5 hours, evaporate the solvent in vacuo and dissolve the residue in ethyl acetate (200 mL). Wash with water, saturated sodium chloride, dry (Mg SO4) and evaporate the solvent in vacuo to give the intermediate N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-oxoethyl-L-serine, methyl ester as a foam (13.6 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428158 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-5c8da73e210d40aaa7b93f90ddc1afb7 |
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| Quellennotiz | uspto-grants-1995_06 |
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