HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7285Erstellt: 23. Oktober 2026
Ethyl Acetate → Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioate
https://huagongshe.com/de/reaction/7285
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | D-Glutamic Acid | HCID 23327 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | Potassium Bicarbonate | HCID 516893 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Dimethyl (2R)-2-{[(benzyloxy)carbonyl]amino}pentanedioate | HCID 86606597 | — |
Reaktionsschritte
Thionyl chloride (30 ml) was added to a cooled solution of D-glutamic acid (33.2 g) in methanol (250 ml) and the mixture subsequently heated under reflux for 16 h. On cooling, the mixture was concentrated under reduced pressure and the residue azeotroped with toluene to give a white solid. This was stirred with ethyl acetate, water and potassium hydrogen carbonate at 0° C. while benzyl chloroformate (30 ml) was added. The mixture was warmed to room temperature and stirred for 5 h. The separated organic phase was washed with water, dried (over magnesium sulphate) and concentrated under reduced pressure to provide a yellow oil. This oil was purified using flash column chromatography (silica, eluting with cyclohexane:ethyl acetate 2:1) to give the title compound (22.45 g) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07084139B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-0d66f2913bdf4cf684ad6583f5f27c4b |
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| Quellennotiz | uspto-grants-2006_08 |
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