HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64453Erstellt: 26. Oktober 2026
Water → methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate
https://huagongshe.com/reaction/64453
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl- | HCID 552336 | — |
| Edukt | (S)-N-Boc-1-(3-bromophenyl)ethylamine | HCID 56971804 | — |
| Katalysator | Zinc(II) fluoride | HCID 10129912 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate | HCID 86713467 | — |
Reaktionsschritte
A mixture of 1 g of tert-butyl[(1S)-1-(3-bromophenyl)ethyl]carbamate, 18 mg of bis(tri-tert-butylphosphine)palladium (0), 180 mg of zinc fluoride, 1 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane, and 10 ml of DMF was stirred at 80° C. overnight and at 100° C. for 5 hours. 25 mg of bis(tri-tert-butylphosphine)palladium (0) and 0.34 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane were added thereto, followed by stirring at 80° C. for 3 days. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 281 mg of methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447090B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-647d358395324543b17b84fbbf089926 |
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| Quellennotiz | uspto-grants-2016_09 |
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