HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 926940Erstellt: 26. Oktober 2026
Bicarbonate Ion → (2R)-2-Phenylcarbonyloxypropyl(2S)-2-(tert-Butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate
https://huagongshe.com/reaction/926940
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bicarbonate Ion | HCID 769 | — |
| Edukt | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Edukt | N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanine | HCID 14217229 | — |
| Edukt | Boc-L-dopa tetrabutylammonium salt | HCID 131728417 | — |
| Lösungsmittel | tert-Butyl methyl ether | HCID 15413 | — |
| Produkt | (2R)-2-Phenylcarbonyloxypropyl(2S)-2-(tert-Butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate | HCID 46899463 | — |
Reaktionsschritte
Boc-Dopa TBA salt 3 (50 g, 93 mmol), bicarbonate-washed (1R)-2-chloroisopropyl benzoate 5 (20 g, 100 mmol), and N-methylpyrrolidinone (NMP) (100 mL) were added to a 250 mL round bottom flask. The mixture was stirred under a nitrogen atmosphere and heated in an oil bath at 100° C. After ca. 72 hrs the reaction was cooled to room temperature, diluted with tert-butyl methylether (MTBE) (1 L), and washed twice with deionized water (2 L, then 1 L). The organic phase was separated, dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated under reduced pressure to provide 35 g (76 mmol) of (2R)-2-phenylcarbonyloxypropyl(2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate 6 as a tan, viscous oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09290445B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-ac6d7a3090f84f31b3a45f1c609b470a |
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| Quellennotiz | uspto-grants-2016_03 |
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