HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1418790Erstellt: 27. Oktober 2026
1-Bromopropane → N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester
https://huagongshe.com/reaction/1418790
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Bromopropane | HCID 7840 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl ester | HCID 7010613 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester | HCID 22940772 | — |
Reaktionsschritte
4.94 g (15 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 5° C. under argon with 0.61 g (15.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 1.91 g (15.5 mmol) of propyl bromide is added, the reaction temperature is allowed to increase to room temperature and it is stirred for another two hours. For working-up, the batch is taken up in ethyl acetate and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05885548 |
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| Quelldatensatz | uspto-grants-1999_03 |
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| ORD ID | ord-1b1b6d4e4479430986678588eb86f835 |
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| Quellennotiz | uspto-grants-1999_03 |
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