HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64432Erstellt: 25. Oktober 2026
Triethylamine → Methyl (S)-3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate
https://huagongshe.com/reaction/64432
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Edukt | (S)-N-Boc-1-(3-bromophenyl)ethylamine | HCID 56971804 | — |
| Edukt | HCID 178418416 | HCID 178418416 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Methyl (S)-3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate | HCID 86713444 | 151,2% |
Reaktionsschritte
To 820 mg of tert-butyl[(1S)-1-(3-bromophenyl)ethyl]carbamate were added 113 mg of 1,3-bis(diphenylphosphino)propane, 62 mg of palladium acetate, 0.84 ml of triethylamine, 8 ml of DMF, and 12 ml of methanol, followed by stirring at room temperature for 1 hour. While stirring at room temperature, carbon monooxide was intaken for 10 minutes, followed by stirring at 80° C. overnight under a carbon monooxide atmosphere. 113 mg of 1,3-bis(diphenylphosphino)propane and 62 mg of palladium acetate were added thereto, followed by stirring at 80° C. overnight. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine 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 577 mg of methyl 3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}benzoate.
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-883b23c1c5814e0b8408008803b23aa6 |
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| Quellennotiz | uspto-grants-2016_09 |
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